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Oak Farms Dairy in Waco Conducts Voluntary Limited Recall of Half Gallon Plastic Bottles of Whole Chocolate Milk, Half Pint Paper Cartons of Whole Chocolate Milk, and Half Pint Paper Cartons of 1% Chocolate Milk Due to Presence of Alkaline Phosphatase in Samples, U.S. Food & Drug Administration (FDA)
Vitalabs, Inc. Issues Voluntary Recall for Specific Lots of Whey Protein Isolate, U.S. Food & Drug Administration (FDA)
RECALL: Pig Ear Dog Chews, FoodSafety.gov
RECALLS: Organic Herbal Tea, FoodSafety.gov
RECALL: Bologna, FoodSafety.gov
CVM Updates - FDA Releases Electronic Submission Tool, eSubmitter, for Use by the Animal Health Industry, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - FDA to Convene Public Hearing on Ensuring the Safety of Imported Foods and Animal Feed, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - New Draft Guidance Available, U.S. Food & Drug Administration (FDA)
FDA, Justice Department take action against McNeil-PPC Inc., U.S. Food & Drug Administration (FDA)
CVM Updates - FDA Advises Veterinarians of Recent Recall of Human Drug, Phenobarbitol, U.S. Food & Drug Administration (FDA)
Enforcement Report for March 9, 2011, U.S. Food & Drug Administration (FDA)
FDA approves Benlysta to treat lupus, U.S. Food & Drug Administration (FDA)
FDA approves Benlysta to treat lupus--First new lupus drug approved in 56 years, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval for Lamivudine and Tenofovir DF Fixed Dose Combination Tablets, 300 mg/300 mg, U.S. Food & Drug Administration (FDA)
RECALL: Ground Beef, FoodSafety.gov
Update of CVM's What's New - Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
REMEDYTEAS Voluntarily Recalls Peppermint Organic Herbal Tea And Organic Herbal Tea Blend Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
FDA Webinar on Tattoos and Permanent Makeup, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Kaletra (lopinavir/ritonavir): Label Change - Serious Health Problems in Premature Babies, FDA MedWatch
McCormick & Company Recalls Golden Dipt® Tempura Seafood Batter Mix Due To Unlabeled Milk Ingredient, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Golden Dipt Tempura Seafood Batter Mix, FoodSafety.gov
Unilever Announces Recall of Skippy® Reduced Fat Peanut Butter Spread Due to Possible Health Risk Limited Recall of 6 Best-If-Used-By Dates, U.S. Food & Drug Administration (FDA)
DeFranco and Sons Recall Bulk and Consumer-packaged In-shell, Hazelnut and Mixed Nut Products Containing Hazelnuts, U.S. Food & Drug Administration (FDA)
FDA: E. coli O157:H7 cases linked to hazelnuts, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - The due date for applying to CVM's 2011 Summer Intern Program "Windows to Regulatory Research" has been extended to March 18, 2011, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval for abacavir sulfate scored tablets for oral suspension, 60 mg, U.S. Food & Drug Administration (FDA)
FDA modifies boxed warning for pulmonary arterial hypertension drug Letairis, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Topamax (topiramate): Label Change - Risk For Development of Cleft Lip and/or Cleft Palate in Newborns, FDA MedWatch
FDA: Risk of oral birth defects in children born to mothers taking topiramate, U.S. Food & Drug Administration (FDA)
Food Co. Recalls Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA expands use of banding system for weight loss, U.S. Food & Drug Administration (FDA)
Garden of Life, LLC. Issues a Voluntary Recall of Vitamin Code Raw Vitamin C Dietary Supplement. Recall is Limited to Raw Vitamin C Only. No Other Garden of Life Products are Involved., U.S. Food & Drug Administration (FDA)
FDA MedWatch - Davol XenMatrix Surgical Graft: Class I Recall - Elevated Endotoxin Levels, FDA MedWatch
FDA MedWatch - Cook Inc., Single, Double, Triple and Five-Lumen Central Venous Catheter Trays, Single and Double Lumen PICC Peripheral Inserted Central Venous Catheter Trays Recall, FDA MedWatch
Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
Enforcement Report for March 2, 2011, U.S. Food & Drug Administration (FDA)
FDA prompts removal of unapproved drugs from market, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Unapproved Cough, Cold, Allergy Products: FDA Prompts Removal From Market, FDA MedWatch
FDA MedWatch - Proton Pump Inhibitor drugs (PPIs): Drug Safety Communication - Low Magnesium Levels Can Be Associated With Long-Term Use, FDA MedWatch
Update of CVM's What's New - The Story of the Center for Veterinary Medicine (video), U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Safety Review update of Abacavir: no statistically significant association seen between myocardial infarction and ABC, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Wellpet LLC Voluntarily Recalls Certain Lots Of Canned Cat Food, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Abacavir - Ongoing Safety Review: Possible Increased Risk of Heart Attack, FDA MedWatch
FDA approves new drug to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
E&J Brandy Announces A Nationwide Recall Of Stainless Steel Flasks Due To Possible Lead Risk, U.S. Food & Drug Administration (FDA)
W H & GROUP, LLC. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
The March 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
FDA approves Edarbi to treat high blood pressure, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Negative Pressure Wound Therapy (NPWT) systems UPDATE, FDA MedWatch
ALLERGY ALERT: Maya Dry Fruit Kachori contains peanuts, FoodSafety.gov
ALLERGY ALERT: Nibble with Gibble's and Kay & Ray's Chips May Contain Soy, FoodSafety.gov
RECALL: Pacific American Fish Roe Capelin, Risk of Botulism, FoodSafety.gov
ALLERGY ALERT: Haddon House Asian Gourmet Cheese Rice Crackers, FoodSafety.gov
Arkansas Firm Recalls Various Meat and Poultry Products Produced Without Inspection, FoodSafety.gov
FDA: Advanced genomic test helps trace sources of foodborne illness outbreak, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Kaletra (lopinavir/ritonavir) Oral Solution label changes related to toxicity in preterm neonates, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Label change for Viracept (nelfinavir): drug-drug interaction information with warfarin, U.S. Food & Drug Administration (FDA)
Urgent Recall on Asian Gourmet Cheese Rice Crackers Which May Contain Undeclared Milk and Undeclared Food Coloring Additives., U.S. Food & Drug Administration (FDA)
Svelte 30 Nutritional Consultants Issues a Voluntary Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
FDA and Georgetown University Medical Center announce partnership, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Approval of zidovudine water-disperable tablets, 100 mg for pediatrics/adults unable to swallow tablets, U.S. Food & Drug Administration (FDA)
Roche Insulin Delivery Systems announces recall of ACCU-CHEK® FlexLink Plus infusion sets, U.S. Food & Drug Administration (FDA)
Consumer Alert: Undeclared Peanuts In Dry Fruit "Kachori", U.S. Food & Drug Administration (FDA)
FDA: U.S. Marshals seize food products at Tennessee company, U.S. Food & Drug Administration (FDA)
Martin's Famous Pastry Shoppe, Inc. Issues Allergy Alert On Undeclared Soy Protein In Certain "Nibble With Gibble's" And Kay And Ray's Branded Products, U.S. Food & Drug Administration (FDA)
Pacific American Fish Co. Recall Shishamo Roe Capelin 4L Due To Potential of C. Botulinum, U.S. Food & Drug Administration (FDA)
Advanced genomic test helps trace sources of foodborne illness outbreak, U.S. Food & Drug Administration (FDA)
Enforcement Report for February 23, 2011, U.S. Food & Drug Administration (FDA)
FDA MedWatch - January 2011 Safety Labeling Changes; 43 products with revisions to Prescribing Information, FDA MedWatch
FDA MedWatch - Extenze Tablets: Recall, FDA MedWatch
BIOTAB NUTRACEUTICALS, INC. Issues a Voluntary Recall of Specific Lots of the Nutritional Supplement EXTENZE (Men's Regular), U.S. Food & Drug Administration (FDA)
FDA permits marketing of first test for most common cause of gastroenteritis outbreaks, U.S. Food & Drug Administration (FDA)
Natural Choice Distribution Company Inc. Voluntarily Recalls Certain Lots Of Fare And Square Sandwiches, Superfresh Sandwiches, And Real Wraps Burritos Due To The Presence Of Undeclared Allergens, U.S. Food & Drug Administration (FDA)
PHOTO - Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
Upsher-Smith Laboratories Announces Expansion of Voluntary Nationwide Recall. Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven® and Oxybutynin, U.S. Food & Drug Administration (FDA)
Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Antipsychotic Drugs: Class Labeling Change - Treatment During Pregnancy and Potential Risk to Newborns, FDA MedWatch
Safety is NO Accident...National Public Health Week April 4-10, 2011, U.S. Food & Drug Administration (FDA)
FDA approves product to prevent bleeding in people with rare genetic defect, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Notice of Extension of Comment Period; Unapproved Animal Drugs, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Warfarin Sodium Tablets (Jantoven), 3mg: Recall - Mislabeled Bottles Containing Higher Dosage, FDA MedWatch
FDA warns against certain uses of asthma drug terbutaline for preterm labor, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Terbutaline: Label Change - Warnings Against Use for Treatment of Preterm Labor, FDA MedWatch
HIV/AIDS Update - Tentative approval of abacavir sulfate Oral Solution, 20 mg/mL, U.S. Food & Drug Administration (FDA)
Upsher-Smith Laboratories Announces The Voluntary Nationwide Recall Of Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles, U.S. Food & Drug Administration (FDA)
Enforcement Report for February 16, 2011, U.S. Food & Drug Administration (FDA)
U.S. Marshals seize Auralgan Otic Solution, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Medtronic SynchroMed II and SynchroMed EL Implantable Infusion Pump and Refill Kits: Class 1 Recall, FDA MedWatch
Prime Choice Foods Corporation Voluntarily Recalls Certain Lots Of Garden Of Eatin'® Multi Grain Tortilla Chips Due To The Presence Of Undeclared Allergens, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Triad Sterile Lubricating Jelly: Recall - Product May Not Be Sterile, FDA MedWatch
FDA seeks to invest in foodborne illness prevention, medical product safety and countermeasures, U.S. Food & Drug Administration (FDA)
FDA finalizes regulation for certain software, hardware used with medical devices, U.S. Food & Drug Administration (FDA)
January, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT EXPANDED: f'realStrawberry Banana Smoothies -- May Contain Peanuts, FoodSafety.gov
f'real® foods Expands Voluntary Recall Of Strawberry Banana Smoothies Due To Potential Peanut Content, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Barbecue Pork Sold in AL, GA, TN, MS, may contain dairy (whey), FoodSafety.gov
ALLERGY ALERT: Essentials, RightFood, other BioSan dietary supplements, may contain soy, FoodSafety.gov
ALLERGY ALERT: H-E-B Frozen Breaded Okra Sold in Texas, may contain dairy (whey), FoodSafety.gov
RECALL: Smoked Salmon sold at The Fresh Market, possible Listeria, FoodSafety.gov
RECALL: Ground Beef Products (Possible E. Coli Contamination), FoodSafety.gov
ALLERGY ALERT: f'real® Strawberry Banana Smoothies may contain peanuts, FoodSafety.gov
ALLERGY ALERT: Frozen Yellow Fin Tuna, FoodSafety.gov
FDA approves first 3-D mammography imaging system, U.S. Food & Drug Administration (FDA)
f'real® foods Issues Voluntary Recall of Strawberry Banana Smoothies Due to Potential Peanut Content, U.S. Food & Drug Administration (FDA)
FDA clears test to help patients with kidney transplants, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - February 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
St James Smokehouse, Inc, Announces Voluntary Recall of Scotch Reserve Whiskey & Honey Smoked Salmon 4oz Retail Packs Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
Neuro Resource Group, Inc. Informs Customers of Important Information about Triad Group's Alcohol Prep Pads, U.S. Food & Drug Administration (FDA)
FDA Webinar on Safety of the Blood Supply, U.S. Food & Drug Administration (FDA)
Enforcement Report for February 9, 2011, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Arstasis One Access System: Class I Recall - Components May Fracture and/or Separate, FDA MedWatch
Are all personal care products regulated as cosmetics?, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Are all personal care products regulated as cosmetics?, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Letter to Veterinarians and Pharmacy Professionals re: SucroMate Equine (deslorelin acetate), U.S. Food & Drug Administration (FDA)
FDA Hepatitis Update - Important information about alcohol prep pads packaged with Pegasys and certain other injection products, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Important information about alcohol prep pads packaged with Fuzeon and certain other injection products, U.S. Food & Drug Administration (FDA)
Pandemic Influenza Evaluation and Capacity Review Tools, U.S. Dept. of Health & Human Services
How do the activities of the USDA FSIS differ from the activities of the FDA Center for Food Safety and Applied Nutrition?, U.S. Food & Drug Administration (FDA)
FDA launches Medical Device Innovation Initiative, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Hydrocodone Bitartrate And Acetaminophen Tablets, Phenobarbital Tablets by Qualitest: Recall - Incorrect Package Labeling, FDA MedWatch
FDA orders postmarket surveillance of certain TMJ implants, U.S. Food & Drug Administration (FDA)
Rouses Markets Voluntarily Recalls Frozen Yellow Fin Tuna Steaks Due To Possible Health Risks, U.S. Food & Drug Administration (FDA)
Watson Announces Important Action Related to Nationwide Recall of Triad Alcohol Prep Products Included in Products, U.S. Food & Drug Administration (FDA)
American Regent Initiates Nationwide Voluntary Recall of Potassium Phosphates Injection, USP 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium 5 mL Single Dose Vial, Lot# 0048 Due to Translucent Visible Particles, U.S. Food & Drug Administration (FDA)
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall Of Hydrocodone Bitartrate And Acetaminophen Tablets, USP 10 MG / 500 MG, NDC 0603-3888-20, 60 Count, Lot Numbers T150G10B, T120J10E And T023M10A And Phenobarbital Tablets, USP 32.4 MG, NDC 0603-5166-32, 1000 Count, Lot Numbers T150G10B, T, U.S. Food & Drug Administration (FDA)
FDA MedWatch - American Regent Injectable Products: Recall - Visible Particulates in Products, FDA MedWatch
HIV/AIDS Update - Reyataz (atazanavir) label revised, adding dosing recommendations for pregnancy and postpartum period, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Merit Prelude Short Sheath Catheter Introducer: Class I Recall - Tip May Detach During Use, FDA MedWatch
CVM Updates - FDA Announces Upcoming Shortage of Vetsulin for Dogs and Cats in the Critical Need Program, U.S. Food & Drug Administration (FDA)
FDA Office of Women's Health eUpdate, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Apple Chipotle Salsa, Maple BBQ Grilling Sauce, & Pumpkin Chipotle Roasting Sauce (contain wheat), FoodSafety.gov
ALLERGY ALERT: Mooney's Kentucky Bourbon Cheese & Valumarket's Beer Cheese Spread (contains soy and fish), FoodSafety.gov
ALLERGY ALERT: Mariegold Baking White Bread and Vallarta Premium White Bread (contain milk), FoodSafety.gov
ALLERGY ALERT: Caesar Dressing (contains eggs), FoodSafety.gov
American Spoon Foods brand Apple Chipotle Salsa, Maple BBQ Grilling Sauce, and Pumpkin Chipotle Roasting Sauce may contain undeclared wheat flour and may put certain consumers at risk for wheat or gluten sensitivities or allergies., U.S. Food & Drug Administration (FDA)
FDA clears first diagnostic radiology application for mobile devices, U.S. Food & Drug Administration (FDA)
Shaping Beauty, Inc. Issues a Voluntary Nationwide Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
American Regent Initiates Nationwide Voluntary Recall of Sodium Thiosulfate Injection, USP 10% (100 mg/mL) 10 mL Single Dose Vials Lot# 0056 Due to Translucent Visible Particles, U.S. Food & Drug Administration (FDA)
FDA approves drug to reduce risk of preterm birth in at-risk pregnant women, U.S. Food & Drug Administration (FDA)
FDA MedWatch - UPDATE: Avandia (rosiglitazone): Information on cardiovascular risks (including heart attack) added to labeling and Medication Guide, FDA MedWatch
Updated: Undeclared Soy And Anchovy Puree In "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread", U.S. Food & Drug Administration (FDA)
Godi International, Corp. Issues a Voluntary Nationwide and International Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement., U.S. Food & Drug Administration (FDA)
Unified Grocers Issues Allergy Alert on Undeclared Milk in Mariegold Baking White Bread (24 oz) and Vallarta Premium White Bread (24 oz), U.S. Food & Drug Administration (FDA)
Tomaso's Issues Allergy Alert On Undeclared Eggs In Caesar Dressing, U.S. Food & Drug Administration (FDA)
FDA reminds health care professionals about safe use of non-sterile alcohol prep pads, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - New Guidance - Target Animal Safety & Effectiveness Protocol Development & Submission, U.S. Food & Drug Administration (FDA)
Magic Valley Fresh Frozen, Inc. Foods Issues Allergy Alert On Undeclared Milk In Breaded Okra, U.S. Food & Drug Administration (FDA)
Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group's Alcohol Prep Products, U.S. Food & Drug Administration (FDA)
Sabor Farms Recalls Four Brands Of Cilantro Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
RECALL: Fresh Cilantro, FoodSafety.gov
FDA MedWatch - B. Braun Outlook 400ES Safety Infusion System, Model Number 621-400ES: Class I Recall - Hardware May Become Unresponsive, FDA MedWatch
RECALL: Horse Feed Distributed in California, Nevada, and Oregon, FoodSafety.gov
RECALL: Jr. Texas JR Taffy pet treat, possible Salmonella, FoodSafety.gov
ALLERGY ALERTS: Ice Cream, Cheese, Veal Ravioli, FoodSafety.gov
The February 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - January 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - two recalls - Family Farm Complete Horse 10 horse feed and Jr. Texas Taffy pet treat, U.S. Food & Drug Administration (FDA)
Publix Issues Voluntary Recall on Ice Cream Containing Undeclared Allergen, U.S. Food & Drug Administration (FDA)
MERRICK PET CARE RECALLS JR TEXAS TAFFY PET TREAT (ITEM # 27077, ALL LOTS UP TO AND INCLUDING 10364) BECAUSE OF POSSIBLE SALMONELLA HEALTH RISK, U.S. Food & Drug Administration (FDA)
Feed Manufacturer Issues Limited Voluntary Recall of a Horse Feed Product Distributed in California, Nevada, and Oregon, U.S. Food & Drug Administration (FDA)
Undeclared Soy in "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread", U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Keebler Fudge Shoppe Jumbo Fudge Sticks sold at convenience stores, FoodSafety.gov
RECALL: All Toxic Waste brand Nuclear Sludge Products, FoodSafety.gov
KEEBLER ISSUES ALLERGY ALERT ON MISLABELED 8-COUNT CARTONS OF FUDGE SHOPPE® JUMBO FUDGE STICKS SOLD AT CONVENIENCE STORES, U.S. Food & Drug Administration (FDA)
Candy Dynamics Expands Recall to all Toxic Waste® brand Nuclear Sludge® Products all flavors and all sizes, U.S. Food & Drug Administration (FDA)
PEEKAY INTERNATIONAL INC. ISSUES ALLERGY ALERT ON UNDECLARED SULFITES IN SWAN GOLDEN RAISINS, U.S. Food & Drug Administration (FDA)
Important information for ARIXTRA® Starter Kit patients regarding Triad Group's alcohol prep products, U.S. Food & Drug Administration (FDA)
Fourth FDA orphan drug designation workshop scheduled for Feb. 28 - March 1, 2011, U.S. Food & Drug Administration (FDA)
ALLERGY ALERTS: Calamari, Corn Pops, Shrimp, Potato Chips, FoodSafety.gov
RECALL: Wide Variety of Salad Greens, Including Organic, Sold on the East Coast, FoodSafety.gov
State Garden, Inc. Announces Voluntary Recall Of Certain Salad Mixes Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
Pfizer Inc. And Progenics Alert Physicians And Patients To Information Related To Triad Group Alcohol Prep Products Included In U.S. RELISTOR Kit Packaging, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Breast Implants: FDA Review Indicates Possible Association With A Rare Cancer, FDA MedWatch
FDA review indicates possible association between breast implants and a rare cancer, U.S. Food & Drug Administration (FDA)
RECALL: Two of Ian's brand Frozen Entrees, FoodSafety.gov
Ian's Voluntarily Recalls Two Products Due To Risk Of Contamination By Listeria Bacteria, U.S. Food & Drug Administration (FDA)
King & Prince Seafood Issues Voluntary Recall Notice On Breaded Calamari Products, U.S. Food & Drug Administration (FDA)
Kanec USA, Inc. Issues a Voluntary Recall of Nite Rider Maximum Sexual Enhancer For Men and STUD Capsules for Men Male Enhancement Herbal Supplement Capsules Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
RECALL: Mama Rose's Con Queso, Hopi Corn Salsa -- Possible Botulism Risk, FoodSafety.gov
Pretzels. Inc. Issues Allergy Alert On Undeclared Milk In Better Made Brand Corn Pops, U.S. Food & Drug Administration (FDA)
FDA approves Viibryd to treat major depressive disorder, U.S. Food & Drug Administration (FDA)
CVM Updates - FDA Announces Availability of the NARMS Strategic Plan, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Fresenius Medical Care CombiSet True Flow Series Hemodialysis Blood Tubing Set with Priming Set and Transducer Protectors: Class I Recall - Potential for Kinking of Arterial Line, FDA MedWatch
Hawaii Business Group Incorporated, Barb's Favorite Recipes, and Ohana Seafoods Recall Barb's Local Style Black Bean Sauce and Ohana Flavors Black Bean Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Mama Rose's Gourmet Foods Recalls Cilantro Con Queso, Garlic Con Queso, Viper Venom Con Queso and Hopi Corn Salsa Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Important Information for Betaseron® (interferon beta 1-b) Consumers Regarding Triad Group's Alcohol Prep Products, U.S. Food & Drug Administration (FDA)
Maine seafood processor enters into consent decree with FDA, U.S. Food & Drug Administration (FDA)
Rich Products Corporation announces nationwide voluntary recall of Sonny's Barbecue Deep Deveined Shrimp, U.S. Food & Drug Administration (FDA)
Barrel O' Fun Snack Foods Co. Issues Allergen Alert on Undeclared Milk Protein in, U.S. Food & Drug Administration (FDA)
Enforcement Report for January 19, 2011, U.S. Food & Drug Administration (FDA)
FDA to improve most common review path for medical devices, U.S. Food & Drug Administration (FDA)
RECALL: Toxic Waste® brand Nuclear Sludge® Chew Bars, FoodSafety.gov
RECALL: Ossie's Schmaltz Herring, FoodSafety.gov
RECALL: Winn-Dixie Beef Patties, OneGreat Hamburgers, FoodSafety.gov
ALLERGY ALERT: Kroger Chocolate Chips Contain Milk, FoodSafety.gov
FDA Approves Head Lice Treatment for Children and Adults, U.S. Food & Drug Administration (FDA)
Commissioner's Fellowship Program, U.S. Food & Drug Administration (FDA)
Federal government obtains permanent injunction against Deltex Pharmaceuticals Inc., U.S. Food & Drug Administration (FDA)
Barry Callebaut USA LLC Issues Allergen Alert on Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips, U.S. Food & Drug Administration (FDA)
Genentech Informs Customers Of Important Information About Triad Groups, U.S. Food & Drug Administration (FDA)
McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products, U.S. Food & Drug Administration (FDA)
MS Fish Corp Issues Alert On Listeria In, U.S. Food & Drug Administration (FDA)
Multaq (dronedarone)- Risk of Severe Liver Injury:Reports include two cases of liver failure leading to liver transplant, FDA MedWatch
December 2010 Safety Labeling Changes: 58 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
Enforcement Report for January 12, 2011, U.S. Food & Drug Administration (FDA)
Candy Dynamics Recalls Toxic Waste® brand Nuclear Sludge® Chew Bars, U.S. Food & Drug Administration (FDA)
FDA seeks to halt processing, distribution at New York juice company, U.S. Food & Drug Administration (FDA)
CVM Updates - January 2011 Update on Feed Enforcement Activities to Limit the Spread of BSE, U.S. Food & Drug Administration (FDA)
Barry Callebaut USA LLC Issues Allergen Alert on Potential Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips, U.S. Food & Drug Administration (FDA)
U.S. Marshals seize dental devices from Florida manufacturer, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Acetaminophen Prescription Products Limited to 325 mg Per Dosage Unit: Drug Safety Communication, FDA MedWatch
FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Webinar Announcement - Question-Based Review - Part III: Sterile Process Validation, U.S. Food & Drug Administration (FDA)
The January 2011 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
Surtex Foods Recalls "Oaxaca String Cheese La Original" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
RECALL: Ground Beef Distributed to Institutions in CA and OR, FoodSafety.gov
FDA MedWatch - Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL): Medication Use Error - Reports of Accidental Overdose, FDA MedWatch
HIV/AIDS Update - Revised Adult HIV Treatment Guidelines available, U.S. Food & Drug Administration (FDA)
AngioScore Incorporated Announces Worldwide Voluntary Field Removal of the AngioSculpt® PTA Scoring Balloon Catheter, 0.018" OTW, balloon sizes: 4.0x20mm, 5.0x20mm, and 6.0x20mm, U.S. Food & Drug Administration (FDA)
La Placita Botanas Mexicanas, Inc. Recalls Wheat Snacks with Chile, Potato Chips with Chile, and Corn Churritos with Chile Because of Possible Contamination with Salmonella, U.S. Food & Drug Administration (FDA)
FDA approves opioid analgesic to help cancer patients manage pain, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval of lamivudine and tenofovir DF 300 mg/300 mg fixed-dose combination, U.S. Food & Drug Administration (FDA)
CVM Updates - CVM Working to Address Shortage of Injectable Iron Dextran - Status Update, U.S. Food & Drug Administration (FDA)
FDA inspects retailers in Miss.; issues warning letters for illegal tobacco sales to minors, U.S. Food & Drug Administration (FDA)
RECALL: Cilantro & Parsley (Wegmans, Boncheff brands) in NY & PA, FoodSafety.gov
ALLERGY ALERT: Beef, Turkey, and Chicken Tamales in CA, OR, WA, FoodSafety.gov
Boncheff Greenhouses, Inc. Recalls For Wegmans Food Markets, Inc., Budwey Markets, Wades Market, Cuba Giant Food Market, And Hegedorn's Cilantro, Curly Parsley, And Italian Parsley Because Of A Possible Health Risk., U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval of lamivudine and zidovudine tablets, 30 mg/60 mg fixed-dose combination, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Triad Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks: Recall Due to Potential Microbial Contamination, FDA MedWatch
FDA MedWatch - Metronidazole Tablets, 250mg: Recall - Underweight Tablets, FDA MedWatch
Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination, U.S. Food & Drug Administration (FDA)
Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets, U.S. Food & Drug Administration (FDA)
FDA launches website to help regulated industries save time, resources, U.S. Food & Drug Administration (FDA)
Enforcement Report for January 5, 2011, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - CVM is now accepting applications for its 2011 Student Summer Intern Program "Windows to Regulatory Research.", U.S. Food & Drug Administration (FDA)
FDA to require substantial equivalence reviews for new tobacco products, U.S. Food & Drug Administration (FDA)
FDA MedWatch - AngioScore Inc., AngioSculpt Percutaneous Transluminal Angioplasty (PTA) Scoring Balloon Catheter OTW 0.018" Platform - Class I Recall, FDA MedWatch
RECALL: Sprouts in WA, OR, ID and AK, FoodSafety.gov
FDA Basics Webinar: State Enforcement Program, U.S. Food & Drug Administration (FDA)
The January 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
SPROUTERS NORTHWEST, INC. RECALLS CLOVER SPROUTS AND CLOVER SPROUT MIXES BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Sprouters Northwest, Inc. Recalls Clover Sprouts and Clover Sprout Mixes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
PRock Marketing, LLC Issues a Voluntary Nationwide Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement., U.S. Food & Drug Administration (FDA)
The Ritedose Corporation Announces the Voluntary Nationwide Recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL Due to Mislabeled Unit Dose Vials, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Albuterol Sulfate Inhalation Solution 0.083%, 3 mL Unit Dose Vials: Recall - Mislabeled Unit Dose Vials, FDA MedWatch
CVM Updates - FDA Announces Minor Use and Minor Species (MUMS) Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Breaded Chicken Wing Products with Egg Distributed to Restaurants, FoodSafety.gov
RECALL: Organic Ground Beef Sold in CA, NJ, NY, NC, WI, WA, FoodSafety.gov
FDA warns consumers not to use Fruta Planta weight loss products, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA warns consumers not to use Fruta Planta weight loss products, U.S. Food & Drug Administration (FDA)
Drive Total Energy Issues a Voluntary Recall of Rock Hard Extreme and Passion Coffee Dietary Supplements, U.S. Food & Drug Administration (FDA)
Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Acetadote (acetylcysteine) Injection: Recall - Particulate Matter Found in a Small Number of Vials, FDA MedWatch
ALLERGY ALERT: Cuernos (Croissants), FoodSafety.gov
ALLERGY ALERT: Teriyaki Beef Jerky with Wheat, FoodSafety.gov
Recall: Fresh Greens, Herbs, Other Produce, FoodSafety.gov
Mexicantown Wholesale Issues Allergy Alert For Undeclared Milk in Cuernos (Croissants), U.S. Food & Drug Administration (FDA)
TINY GREENS ORGANIC FARM FOOD CO. RECALLS PRODUCT BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
Enforcement Report for December 29, 2010, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Arrow Intra-Aortic Balloon (IAB) Catheter Products: Class 1 Recall - Catheters can become Stuck in the Sheath, FDA MedWatch
J&D Produce Announces Precautionary, Voluntary Recall Of Fresh Greens, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Sodium Bicarbonate Injection, USP, 7.5% and 8.4%, 50 mL Single Dose Vials - Recall Due to Particulates in Some Vials, FDA MedWatch
ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter, U.S. Food & Drug Administration (FDA)
American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
ev3 NanoCross .014" OTW PTA Dilatation Catheter: Class I Recall - Potential for cracking or breaking, FDA MedWatch
FDA: Don't Eat Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
Brand Castle, LLC Issues Allergy Alert On Undeclared Egg In Icing Of Licensed Rice Krispies Treats Holiday Village Kit Distributed Through Michaels Retail Stores Only, U.S. Food & Drug Administration (FDA)
American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial, U.S. Food & Drug Administration (FDA)
Whole Foods Market Announces A Recall Of Products Which Were Produced By Rolf's Patisserie In Seven States In The Midwest Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
Whole Foods Market Announces A Recall For Ginger Bread Houses Which Were Produced By Rolf's Patisserie In Twenty-Three States Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
Abbott Diabetes Care Announces Recall of Certain Lots of Precision Xtra®, Precision Xceed Pro®, MediSense® Optium[TM], Optium[TM], OptiumEZ and ReliOn® Ultima Blood Glucose Test Strips in the United States and Puerto Rico, U.S. Food & Drug Administration (FDA)
JFC International Inc. Recalls "Frozen Capelin" Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
South Florida Bakery Issues Recall for Publix Bakery Coconut Macaroons (Coquitos), U.S. Food & Drug Administration (FDA)
FDA: Rolf's Patisserie recalling all desserts made after November 1, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA: Rolf's Patisserie recalling all desserts made after November 1, U.S. Food & Drug Administration (FDA)
Dexamethasone Sodium Phosphate Injection, 4 mg/mL, 30 mL Multiple Dose Vial: Recall due to Particulates in Product, FDA MedWatch
FDA MedWatch - Fruta Planta: Public Notification - Undeclared Drug Ingredient, FDA MedWatch
FDA MedWatch - RockHard Weekend, Pandora: Recall - Undeclared Drug Ingredient, FDA MedWatch
HIV/AIDS Update - New Intelence (etravirine) dosage approved, U.S. Food & Drug Administration (FDA)
Pfizer To Recall One Lot Of Lipitor In The U.S., U.S. Food & Drug Administration (FDA)
RockHard Laboratories Issues a Voluntary Recall of Specific Lots of the Dietary Supplements RockHard Weekend and Pandora, U.S. Food & Drug Administration (FDA)
FDA: Gardasil approved to prevent anal cancer, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA: Gardasil approved to prevent anal cancer, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Recombinant Human Growth Hormone (somatropin): Ongoing Safety Review - Possible Increased Risk of Death, FDA MedWatch
Shining a Light on Insurance Companies, HealthCare.gov
FDA announces recall of Abbott glucose test strips, U.S. Food & Drug Administration (FDA)
RECALLS: Frozen capelin fish and, FoodSafety.gov
FDA MedWatch - Abbott Glucose Test Strips: Recall - False Low Blood Glucose Results, FDA MedWatch
IMPF Voluntarily Recalls Dips & Spreads because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Enforcement Report for December 22, 2010, U.S. Food & Drug Administration (FDA)
Secretary of Health and Human Services Announces 2011 Healthy Living Innovation Awards, U.S. Food & Drug Administration (FDA)
Whole Foods Market Announces Cheese Recall For Products In Three Western States And Washington, D.C. Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
JFC International Inc Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Fresenius Kabi LLC, Red Blood Cell (RBC) Exchange Sets used on AS104 Blood Cell Separation Devices: Class I Recall, FDA MedWatch
HHS and Walgreens Announce New Effort Aimed at Addressing Health Disparities in Flu Vaccination, U.S. Dept. of Health & Human Services
Kroger Recalls Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
YNOT FOODS INC. Issues Allergy Alert on Undeclared Milk and Soybean in Upsides[TM] Orzo Toscano, 6/2.5lb, U.S. Food & Drug Administration (FDA)
Tofutti Brands Inc. Announces Updated Information for Recall of 25 Pallets of Yours Truly Frozen Dessert Cones Due to Possible Trace Level Milk Contamination, U.S. Food & Drug Administration (FDA)
U.S. Food & Drug Administration (FDA) BadAd Update, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Kroger Recalls Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - NARMS Retail Meat Annual Report, 2008, U.S. Food & Drug Administration (FDA)
FDA: Consumers should not eat Sally Jackson cheese due to risk of Escherichia coli O157:H7, U.S. Food & Drug Administration (FDA)
RECALL: All Sally Jackson Cheese, FoodSafety.gov
FDA MedWatch - Anzemet (dolasetron mesylate): Drug Safety Communication - Reports of Abnormal Heart Rhythms, FDA MedWatch
Sally Jackson Cheese Recalls All Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Avastin (bevacizumab): Process for Removal of Breast Cancer Indication Begun, FDA MedWatch
FDA Hepatitis Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination, U.S. Food & Drug Administration (FDA)
FDA begins process to remove breast cancer indication from Avastin label, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - New Issue of FDA Veterinarian Newsletter!, U.S. Food & Drug Administration (FDA)
Enforcement Report for December 15, 2010, U.S. Food & Drug Administration (FDA)
FDA: Tainted products marketed as dietary supplements potentially dangerous, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Brinkman's Gourmet Barbecue Sauce, FoodSafety.gov
Update of CVM's What's New - December 2010 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
Brinkman Turkey Farms Inc. Issues Allergy Alert On Undeclared Soy And Milk In "Brinkman's Gourmet Barbecue Sauce"., U.S. Food & Drug Administration (FDA)
FDA says Tessalon liquid cough capsules pose risk for young children, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Tessalon (benzonatate): Drug Safety Communication - Potential for Accidental Ingestion by Children, FDA MedWatch
FDA MedWatch - Rolaids Extra Strength Softchews, Rolaids Extra Strength plus Gas Softchews, Rolaids Multi-Symptom plus Anti-Gas Softchews: Recall - Foreign Materials in Products, FDA MedWatch
Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
RECALL: Walnuts with Salmonella, FoodSafety.gov
H1N1 Vaccine Safe and Induces Robust Immune Response in People with Asthma, U.S. Dept. of Health & Human Services
U.S. Food & Drug Administration (FDA) New FDA Basics Summary Metrics, U.S. Food & Drug Administration (FDA)
Tropical Nut & Fruit of Charlotte, NC Announces a Nationwide Voluntary Recall of Walnut Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
McNeil Consumer Healthcare Announces Voluntary Recall Of All Lots Of Rolaids® Extra Strength Softchews, Roldaids® Extra Strength Plus Gas Softchews, And Roldaids® Multi-Symptom Plus Anti-Gas Softchews Sold In The United States, U.S. Food & Drug Administration (FDA)
U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in New Mexico, U.S. Food & Drug Administration (FDA)
Updated: With Table - Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled., U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - New labeling approved for Prezista (darunavir), U.S. Food & Drug Administration (FDA)
Toffutti Brands Inc. Announces Recall Of 25 Pallets Of Yours Truly Frozen Dessert Cones Due To Possible Trace Level Milk Contamination, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Man Up Now Capsules: Consumer Warning - Undeclared Drug Ingredient, FDA MedWatch
ALLERGY ALERT: Sauteed Chicken Products Sold to Restaurants in CA and HI, FoodSafety.gov
FDA MedWatch - Reese Pharmaceutical Company OTC Products: Recall - Mislabeled Guaifenesin Tablets, FDA MedWatch
Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled., U.S. Food & Drug Administration (FDA)
FDA warns consumers to avoid Man Up Now capsules, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update -New labeling for Zerit capsules and Zerit for oral solution, U.S. Food & Drug Administration (FDA)
Mojave Foods Corporation Initiates Recall Due to Possible Health Risk from Walnut Ingredient, U.S. Food & Drug Administration (FDA)
CVM Updates - CVM Reports on Antimicrobials Sold or Distributed for Food-Producing Animals, U.S. Food & Drug Administration (FDA)
RECALLS: Cilantro, Pork Products, Dried Fish, FoodSafety.gov
FDA issues guidance on public comment procedures at advisory committee meetings, U.S. Food & Drug Administration (FDA)
Pablo's Produce, Inc. Recalls One Lot of Cilantro because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Enforcement Report for December 8, 2010, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Penumbra System Reperfusion Catheter 032: Class I Recall Due to Manufacturing Error, FDA MedWatch
November 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
A Flu Vaccine that Lasts: NIH Scientists Consider Prospects for a Universal Influenza Vaccine, U.S. Dept. of Health & Human Services
Presidential Proclamation--National Influenza Vaccination Week, U.S. Dept. of Health & Human Services
S&S Food Inc. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
The December 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
Wisconsin Business Recalls Smoked Fish Spread; May Be Contaminated With Listeria, U.S. Food & Drug Administration (FDA)
National Influenza Vaccination Week to be held December 5-11, 2010, U.S. Dept. of Health & Human Services
Seasonal Flu and 2009 H1N1 Flu Vaccination Coverage Among Pregnant Women, 2009--10 Flu Season, U.S. Dept. of Health & Human Services
Lobby Shoppes, Inc. Issues An Allergy Alert On Milk And Soy Products In "Cheese Popcorn, Chicago Triple Mix Popcorn And Caramel Corn", U.S. Food & Drug Administration (FDA)
California Firm Recalls Chicken Tamales Due To Mislabeling and an Undeclared Allergen, FoodSafety.gov
RECALL: Bumble Bee Chicken Salad, FoodSafety.gov
Intelli Health Products, Issues an Expansion to All Lots of their Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
FDA Hepatitis Update - FDA seeking new members with Hep C experience for its Antiviral Drugs Advisory Committee, U.S. Food & Drug Administration (FDA)
CVM Updates - FDA Approves First Drug to Prevent Life Threatening Disease in Horses, U.S. Food & Drug Administration (FDA)
RECALL: NY Gourmet Salads, FoodSafety.gov
Update of CVM's What's New - New Guidance - Residual Solvents in Animal Drug Products, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Approval of rapid INSTI[TM] HIV-1 Antibody Test, U.S. Food & Drug Administration (FDA)
Recall of Mylanta and Alternagel Liquid Products, U.S. Food & Drug Administration (FDA)
Special Edition OWH eUpdate, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - November 2010 Green Book Update, U.S. Food & Drug Administration (FDA)
RECALL: Frontier and Whole Foods Nutmeg, FoodSafety.gov
Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Nutmeg, U.S. Food & Drug Administration (FDA)
Enforcement Report for December 1, 2010, U.S. Food & Drug Administration (FDA)
B. Braun addEASE Binary Connector: Class I Recall -Stopper Fragments May Enter Bag, FDA MedWatch
ALLERGY ALERT: Golden Dipt® Fry Easy All-Purpose Batter, FoodSafety.gov
The December 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
McCormick & Company Recalls Golden Dipt® Fry Easy All-Purpose Batter Due To Unlabeled Egg Ingredient, U.S. Food & Drug Administration (FDA)
FDA Permits Wright County Egg to begin shipping shell eggs to consumers, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 60 mg, U.S. Food & Drug Administration (FDA)
FDA Office of Minority Health Website is live, U.S. Food & Drug Administration (FDA)
Recall of ROLAIDS® Extra Strength Softchews, U.S. Food & Drug Administration (FDA)
Recall of Tylenol Cold Liquid Products, U.S. Food & Drug Administration (FDA)
Recall of Children's BENADRYL® Allergy FASTMELT® Tablets and Junior Strength MOTRIN® Caplets, U.S. Food & Drug Administration (FDA)
FDA MedWatch - HiRes 90K Cochlear Implant Device: Recall - Malfunction, FDA MedWatch
Advanced Bionics Announces Voluntary Recall Of The Hires 90k Cochlear Implant, U.S. Food & Drug Administration (FDA)
Bravo Farms announces cheese recall, some products sold under Whole Foods Market label in 5 Western states, U.S. Food & Drug Administration (FDA)
WalkMed Infusion Issues Nationwide Recall of Triton Pole Mount Infusion Pumps, U.S. Food & Drug Administration (FDA)
Enforcement Report for November 24, 2010, U.S. Food & Drug Administration (FDA)
RECALL: Organic Dark Chocolate Squares, FoodSafety.gov
RECALL: Bravo Farms Recalls All Cheese, FoodSafety.gov
Bravo Farms Cheese Recall, U.S. Food & Drug Administration (FDA)
Artisan Confections Recalls Dagoba new moon™ Rich Dark Chocolate 74% Cacao 0.32-Ounce Squares Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Updated Minor Use Minor Species Designations List, U.S. Food & Drug Administration (FDA)
FDA Basics Webinar: Melamine: The Cause of the Pet Food and Infant Formula Recalls, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - FDA Basics Webinar: Melamine: The Cause of the Pet Food and Infant Formula Recalls, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Micromedics, Inc. Surgical Sealant Dispensers, Nasal Septal Buttons, and Otological Ventilation Tubes: Class 1 Recall-Weak or Open Seals, FDA MedWatch
KRUNCHERS! INC. RECALLS 18 CASES OF JAYS ORIGINAL POTATO CHIPS BECAUSE OF UNDECLARED MILK ALLERGEN, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Krunchers! Inc. Recalls 18 Cases Of Jays Original Potato Chips Because Of Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Vigor-25: Undeclared Drug Ingredient - Sold as Natural Dietary Supplement, FDA MedWatch
FDA warns consumers not to use Vigor-25, U.S. Food & Drug Administration (FDA)
Interim Guidance on the Use of Influenza Antiviral Agents During the 2010-2011 Influenza Season, U.S. Dept. of Health & Human Services
FDA MedWatch - Propoxyphene: Withdrawal - Risk of Cardiac Toxicity, FDA MedWatch
Xanodyne agrees to withdraw propoxyphene from the U.S. market, U.S. Food & Drug Administration (FDA)
FDA approves Xgeva to help prevent cancer-related bone injury, U.S. Food & Drug Administration (FDA)
NIH Experts Describe Influenza Vaccines of the Future, U.S. Dept. of Health & Human Services
Enforcement Report for November 17, 2010, U.S. Food & Drug Administration (FDA)
The Great American Smokeout, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Needleless Pre-filled Glass Syringes: Stakeholder Advisory - Compatibility Problems with Needleless Intravenous Access Systems, FDA MedWatch
Del Bueno Recalls Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA Warning Letters issued to four makers of caffeinated alcoholic beverages, U.S. Food & Drug Administration (FDA)
Liz Lovely Issues Voluntary Recall on Products Containing Chocolate Due to Undeclared Dairy from Chocolate Supplier, U.S. Food & Drug Administration (FDA)
Allergy Alert: Dried Taro with Sulfites, FoodSafety.gov
NIH Scientists Explore 1510 Influenza Pandemic and Lessons Learned, U.S. Dept. of Health & Human Services
S&M (U.S.A) Enterprise Corp Issues Alert on Undeclared Sulfites in Grow Grove Notes Brand Dried Taro, U.S. Food & Drug Administration (FDA)
FDA launches initiative to develop innovative external defibrillators, U.S. Food & Drug Administration (FDA)
FDA approves new treatment option for late-stage breast cancer, U.S. Food & Drug Administration (FDA)
FDA Urges Consumers to be 'Smart' about Antibiotic Use, U.S. Food & Drug Administration (FDA)
RECALL: Costco Cheese Recalls, FoodSafety.gov
RECALL: Smoked Turkey Breast Products, FoodSafety.gov
Voluntary Recall of Bravo Farms Dutch Style Gouda Cheese Due to Health Risk, U.S. Food & Drug Administration (FDA)
Gorgonzola Cheese Sold at Costco Recalled Due to Contamination With E.coli O157:H7, U.S. Food & Drug Administration (FDA)
DPI Specialty Foods Recalls Mauri Brand Gorgonzola Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Sigma Spectrum Infusion Pump Model 35700: Class 1 Recall: Risk of Over-Infusion, FDA MedWatch
October 2010 Safety Labeling Changes: 34 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
RECALL: Mauri Gorgonzola cheese sold at Costco in Colorado, FoodSafety.gov
Enforcement Report for November 10, 2010, U.S. Food & Drug Administration (FDA)
FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7, U.S. Food & Drug Administration (FDA)
FDA Approves Egrifta to Treat Lipodystrophy in HIV Patients, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Approval of Egrifta to treat lipodystrophy, U.S. Food & Drug Administration (FDA)
Pharmaceutical Company Lawyer Charged with Obstruction and Making False Statements, U.S. Food & Drug Administration (FDA)
FDA MedWatch - VITEK 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam (TZP): Recall - Incorrect Test Results Observed, FDA MedWatch
FDA: Majority of drug and biological product makers meeting postmarketing requirements and commitments, U.S. Food & Drug Administration (FDA)
Cal-Maine Foods. Inc. Updates Voluntary Egg Recalls Information, U.S. Food & Drug Administration (FDA)
FDA working to prevent radiation overdoses during CT scans, U.S. Food & Drug Administration (FDA)
Allergy Alert: Fresh & Easy Ginger Spice Cookie Dough, FoodSafety.gov
RECALL: Eggs, FoodSafety.gov
RECALL: Products Containing Cilantro, FoodSafety.gov
RECALL: Trader Joe's Chicken Pasta Salad, FoodSafety.gov
RECALL: Apple Cider, FoodSafety.gov
Update of CVM's What's New - Registration delayed until November 10: AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
HRSA and FDA Present Health Education Awards, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Triton Pole Mount Infusion Pump by WalkMed: Recall - Potential Door Open Alarm Problem, FDA MedWatch
Cal-Maine Foods, Inc. Conducts Voluntary Egg Recall, U.S. Food & Drug Administration (FDA)
Orval Kent Food Company, Inc Voluntarily Recalls Products Containing Cilantro Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
WalkMed Infusion Issues Nationwide Recall of Triton Infusion Pump, U.S. Food & Drug Administration (FDA)
Baugher Enterprise, Inc. Recalls Baugher's Apple Cider Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Carefusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall, U.S. Food & Drug Administration (FDA)
FDA, State of Maryland, and Baugher Enterprise warn consumers to avoid Baugher's Apple Cider, U.S. Food & Drug Administration (FDA)
RECALLS: Meat and Poultry Products in Illinois and New York, FoodSafety.gov
RECALL: Unpasteurized Apple Cider, FoodSafety.gov
The November 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
DHMH Issues Consumer Alert Regarding Recall of Baugher's Apple Cider, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Registration Opens November 8: AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese, U.S. Food & Drug Administration (FDA)
FDA clears Cymbalta to treat chronic musculoskeletal pain, U.S. Food & Drug Administration (FDA)
ALERT: FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese, FoodSafety.gov
FDA MedWatch - Hospira Symbiq One-Channel and Two-Channel Infusers: Class I Recall - Motor Encoder Failures, FDA MedWatch
Beaver Street Fisheries, Inc Voluntarily Recalls Tuna due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h, U.S. Food & Drug Administration (FDA)
Intelli Health Products, Issues a Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
FDA, USDA, Cornell University announce alliance for produce safety, U.S. Food & Drug Administration (FDA)
FDA reclassifies certain digital mammography devices today, U.S. Food & Drug Administration (FDA)
Enforcement Report for November 3, 2010, U.S. Food & Drug Administration (FDA)
New Study Re-examines Bacterial Vaccine Studies Conducted During 1918 Influenza Pandemic, U.S. Dept. of Health & Human Services
MedSun Update, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - October 2010 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Octopus Nuvo Tissue Stabilizer: Recall - Potential for Device Fracture, FDA MedWatch
FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall, U.S. Food & Drug Administration (FDA)
FDA, University of Rochester announce partnership for new drug products, U.S. Food & Drug Administration (FDA)
FDA approves new indication for Afinitor, U.S. Food & Drug Administration (FDA)
New Video for Women with Diabetes, U.S. Food & Drug Administration (FDA)
Kosher First LLC. Issues Alert on Listeria in Tuv Taam Salads Nova Lox Salad, U.S. Food & Drug Administration (FDA)
FDA Approves Teflaro for Bacterial Infections, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Heparin Sodium (B. Braun): Recall - Trace Contaminant, FDA MedWatch
B. Braun Voluntarily Recalls Seven Lots of Heparin Manufactured in 2008 Due to Supplier-Initiated Recall of Heparin Active Pharmaceutical Ingredient (API), U.S. Food & Drug Administration (FDA)
NOAA and FDA Announce Chemical Test for Dispersant in Gulf Seafood;, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Methotrexate Injection, 50mg/2mL and 250mg/10mL Vials: Recall - Presence of Glass Particulates, FDA MedWatch
FDA approves Latuda to treat schizophrenia in adults, U.S. Food & Drug Administration (FDA)
Sandoz initiates voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Methotrexate Injection, USP due to the presence of glass particulates, U.S. Food & Drug Administration (FDA)
FDA approves additional medical indication for Sprycel, U.S. Food & Drug Administration (FDA)
RECALL: Autentico Pork Skins & Pork Products in CA, FoodSafety.gov
Enforcement Report for October 27, 2010, U.S. Food & Drug Administration (FDA)
bioMérieux, Inc. Issues Urgent Product Correction for VITEK® 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam, U.S. Food & Drug Administration (FDA)
U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in Georgia, U.S. Food & Drug Administration (FDA)
CVM Updates - FDA Announces Addition of Boxed Warning to METACAM® (meloxicam) Labels, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Safe Animal Feed Video Available, U.S. Food & Drug Administration (FDA)
FDA awards $18.5 million in grants for food and feed safety, U.S. Food & Drug Administration (FDA)
Federal government takes action against Tennessee food distributor, U.S. Food & Drug Administration (FDA)
Federal Government has seized Tri-Med Labs drug products, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - FY 2011 Nationwide Assignment to Collect and Analyze Samples of Direct-Human-Contact Feed for Salmonella, U.S. Food & Drug Administration (FDA)
FDA laboratory receives accreditation, U.S. Food & Drug Administration (FDA)
RECALL: Tomi Dried Seafood Products, Botulism Risk, FoodSafety.gov
ALLERGY ALERT: Nestle Raisinets, FoodSafety.gov
RECALL: Market Pantry Beef Sticks, FoodSafety.gov
Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns, FoodSafety.gov
Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland's Teething Tablets to Address Manufacturing Process, U.S. Food & Drug Administration (FDA)
Nestle® USA Issues Allergen Alert on Single Production Code of Nestle® Raisinets® Fun Size Bags, U.S. Food & Drug Administration (FDA)
DSHS Orders Sangar Produce to Close, Recall Products, U.S. Food & Drug Administration (FDA)
Hyland's Teething Tablets may pose a risk to children, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Western Milling LLC Voluntarily Recalls Universal Turkey and Kruse G.B. Turkey Grower Feeds Because of Possible Health Risk to Animals, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Hyland's Teething Tablets: Recall - Risk of Harm to Children, FDA MedWatch
HIV/AIDS Update - Invirase (saquinavir) labels updated with important risk information about abnormal heart rhythms, U.S. Food & Drug Administration (FDA)
2010-2011 Seasonal Influenza (Flu) Vaccine Safety, U.S. Dept. of Health & Human Services
Western Milling LLC Voluntarily Recalls Universal Turkey and Kruse G.B. Turkey Grower Feeds Because of Possible Health Risk to Animals, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Fentanyl Transdermal System: Recall - Potential for Active Ingredient to Release Faster Than Specified, FDA MedWatch
FDA Heightens Focus on Retail Food Safety, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA heightens focus on retail food safety, U.S. Food & Drug Administration (FDA)
Foremost Foods International, Inc. Issues Recall on Certain Tomi Dried Seafood Products, U.S. Food & Drug Administration (FDA)
Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h, U.S. Food & Drug Administration (FDA)
Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan, FoodSafety.gov
FDA MedWatch - Invirase (saquinavir): Label Change - Risk of Abnormal Heart Rhythm, FDA MedWatch
New Label Changes for Commonly Prescribed HIV Drug Invirase, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - additional Veterinary Medicine Advisory Committee materials posted, U.S. Food & Drug Administration (FDA)
Enforcement Report for October 20, 2010, U.S. Food & Drug Administration (FDA)
September 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
FDA MedWatch - GnRH Agonists: Label Change - Increased Risk of Diabetes and Cardiovascular Disease (Update), FDA MedWatch
FDA: Include warnings on risk for class of prostate cancer drugs, U.S. Food & Drug Administration (FDA)
FDA approves Pradaxa to prevent stroke in people with atrial fibrillation, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update -Tentative approval of lamivudine and stavudine Fixed Dose Combination tablets, 150/300 mg, U.S. Food & Drug Administration (FDA)
FDA Basics Webinar: Food Emergency Response Network (FERN), U.S. Food & Drug Administration (FDA)
FDA MedWatch - Tylenol 8 Hour Caplets 50 Count: Recall - Uncharacteristic musty or moldy odor, FDA MedWatch
McNeil Consumer Healthcare Announces Voluntary Recall of One Product Lot of TYLENOL® 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Presentations from the September 20, 2010 Veterinary Medicine Advisory Committee Meeting, U.S. Food & Drug Administration (FDA)
FDA Provides Update on LASIK Quality of Life Collaboration Project Status, U.S. Food & Drug Administration (FDA)
FDA Authorizes Hillandale Farms to Begin Shipping Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
FDA Issues Warning Letter to Wright County Egg, U.S. Food & Drug Administration (FDA)
FDA Hepatitis Update - New Baraclude (entecavir) Tablets and Oral Solution dosing regimen for chronic hepatitis B (HBV) and decompensated liver disease, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Pre-Registration Notice: AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
**CONSUMER ALERT** Pats Exotic Beverage Recalls "Carrot Juice" Beverage, "Carrot Beet" Beverage, "Carrot Lime" Beverage and "Cucumber" Beverage Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
RECALL: Frozen Green Pea Products Sold at Kroger & Walmart, FoodSafety.gov
The Pictsweet Company Announces a Voluntary Recall of Frozen Green Peas Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA approves Botox to treat chronic migraine, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- FDA approves Botox to treat chronic migraine, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Excelsior Medical 5 ml Fill in 6 cc Prefilled Saline Flush Syringes: Recall - Potential Loss of Sterility, FDA MedWatch
FDA MedWatch - CareFusion Corporation Alaris PC Units (Model 8015): Recall - Potential for Delay or Interruption of Therapy, FDA MedWatch
ALLERGY ALERT: Breaded Okra, FoodSafety.gov
- <Possible follow-ups>
- ALLERGY ALERT: Breaded Okra, FoodSafety.gov
CVM Updates - FDA Announces Letter to Industry on Marketing of Animal Food Substances as Generally Recognized As Safe (GRAS), U.S. Food & Drug Administration (FDA)
The Pictsweet Company Issues Allergy Alert On Undeclared Milk In 32 Ounce Clear Bag Breaded Okra, U.S. Food & Drug Administration (FDA)
Excelsior Medical Recall of 5 ml Fill in 6 cc Prefilled Saline Flush Syringes Classified as a Class I Recall, U.S. Food & Drug Administration (FDA)
FDA participates in 'International Internet Week of Action', U.S. Food & Drug Administration (FDA)
FDA MedWatch - Chelation Products: Unapproved Over-the-Counter Drugs - Consumer Warning, FDA MedWatch
FDA Determines Knee Device Should Not Have Been Cleared for Marketing, U.S. Food & Drug Administration (FDA)
FDA issues warnings to marketers of unapproved 'chelation' products, U.S. Food & Drug Administration (FDA)
Government takes action against Montana drug manufacturer, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Cumulative Veterinary Adverse Drug Experience (ADE) Reports - Updated September 30, 2010, U.S. Food & Drug Administration (FDA)
Enforcement Report for October 13, 2010, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Bisphosphonates (Osteoporosis Drugs): Label Change - Atypical Fractures Update, FDA MedWatch
FDA: Possible increased risk of thigh bone fracture with bisphosphonates, U.S. Food & Drug Administration (FDA)
FDA schedules third orphan drug workshop for Nov. 4-5, 2010, U.S. Food & Drug Administration (FDA)
FDA approves injectable drug to treat opioid-dependent patients, U.S. Food & Drug Administration (FDA)
RECALL: BLUE brand dog food, FoodSafety.gov
RECALL: "La Nuestra" Mamey Ice Cream, FoodSafety.gov
Update of CVM's What's New - Blue Buffalo Company, Ltd. Recalls Limited Production Code Dates of Dry Dog Food Because of Possible Excess Vitamin D, U.S. Food & Drug Administration (FDA)
LIPITOR Recall Information, U.S. Food & Drug Administration (FDA)
Blue Buffalo Company, Ltd. Recalls Limited Production Code Dates of Dry Dog Food Because of Possible Excess Vitamin D, U.S. Food & Drug Administration (FDA)
Influenza Activity - United States and Worldwide, June 13--September 25, 2010, U.S. Dept. of Health & Human Services
Influenza Vaccination Coverage among Children Aged 6-23 Months - U.S., 2008-09 Influenza Season, U.S. Dept. of Health & Human Services
Seasonal Flu Information for Businesses and Employees, U.S. Dept. of Health & Human Services
Final Estimates for 2009-10 Seasonal Influenza and Influenza A (H1N1) 2009 Monovalent Vaccination Coverage - U.S., August, 2009 through May, 2010, U.S. Dept. of Health & Human Services
RECALL: Smoked Fish, FoodSafety.gov
Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Mamey Ice Cream Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
D & M Smoked Fish, Inc. is Recalling Specific Lots of Haifa Smoked Fish Brand Products Sold Between August 10, 2010 and September 3, 2010 Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Slimming Beauty Bitter Orange Slimming Capsules: Undeclared Drug Ingredient, FDA MedWatch
FDA MedWatch - Meridia (sibutramine): Market Withdrawal Due to Risk of Serious Cardiovascular Events, FDA MedWatch
Abbott Laboratories agrees to withdraw its obesity drug Meridia, U.S. Food & Drug Administration (FDA)
FDA: Potentially harmful stimulant found in Slimming Beauty capsules, U.S. Food & Drug Administration (FDA)
Gaspari Nutrition Nutrition Issues a Voluntary Nationwide Recall of Novedex XT, a Product Marketed as a Dietary Supplement Containing ATD, U.S. Food & Drug Administration (FDA)
Living Foods Inc. Initiates a Voluntary Market Withdrawal of Alfalfa Sprouts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
RECALL: Alfalfa Sprouts, FoodSafety.gov
- <Possible follow-ups>
- Recall: Alfalfa Sprouts, FoodSafety.gov
- RECALL: Alfalfa Sprouts, FoodSafety.gov
FDA seeks to stop juice company's processing, distribution, U.S. Food & Drug Administration (FDA)
Enforcement Report for October 6, 2010, U.S. Food & Drug Administration (FDA)
FDA awards $904,000 to Pan American Health Organization for information 'hub', U.S. Food & Drug Administration (FDA)
FDA Issues Regulatory Science Report, U.S. Food & Drug Administration (FDA)
FDA Basic Video: Margaret Oeller (Video), U.S. Food & Drug Administration (FDA)
How does FDA plan to enforce the restrictions on promotion and advertising established by the Tobacco Control Act?, U.S. Food & Drug Administration (FDA)
FDA Basic Video: Diane Murphy Discusses Vaccines (Video), U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: White bread with nuts not listed on the label, FoodSafety.gov
Learn More about New Health Care Benefits - HealthCare.Gov, U.S. Food & Drug Administration (FDA)
Lucerne Foods Voluntarily Recalls Oregon Western Hazelnut Bread Sold at Safeway and WinCo stores in 12 States Due to Undeclared Nut Content, U.S. Food & Drug Administration (FDA)
FDA Hepatitis Update - Approval Pathway for Biosimilar and Interchangeable Biological Products Public Meeting Nov. 2-3, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Approval Pathway for Biosimilar and Interchangeable Biological Products, FDA Public Meeting, U.S. Food & Drug Administration (FDA)
FDA awards nearly $3 million for TB research, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - FDA's Animal Feed Safety System (AFSS) Project Plans Update #7, U.S. Food & Drug Administration (FDA)
The October 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
Q and A: Vaccine Selection for the 2010-2011 Influenza Season, U.S. Dept. of Health & Human Services
FDA schedules public hearing on Biologics Price Competition and Innovation Act, U.S. Food & Drug Administration (FDA)
Rising Dough Bakery Issues Allergy Alert on Undeclared Walnuts in the Rising Dough Brand Individual Wrapped Cranberry Muffins, U.S. Food & Drug Administration (FDA)
Insurer Pricing and Denial Rates Now on HealthCare.gov, HealthCare.gov
HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 300 mg, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Hostess® Mini Muffins (Chocolate Chip variety), FoodSafety.gov
CVM Updates - CVM Announces Availability of Online Pet Pharmacy Brochure through Pueblo, Colorado, U.S. Food & Drug Administration (FDA)
Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen, U.S. Food & Drug Administration (FDA)
FDA Orders Halt to Marketing of Unapproved Single-Ingredient Oral Colchicine, U.S. Food & Drug Administration (FDA)
Enforcement Report for September 29, 2010, U.S. Food & Drug Administration (FDA)
BARDA Funds Development of Next-Generation Portable Ventilators, U.S. Dept. of Health & Human Services
The October 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
Health Requirements and Recommendations for Travel to Saudi Arabia During the 2010 Hajj: Information for U.S. Travelers, U.S. Dept. of Health & Human Services
FDA MedWatch - Infant sleep positioners: Consumer Warning - Risk of Suffocation, FDA MedWatch
Deaths prompt CPSC, FDA warning on infant sleep positioners, U.S. Food & Drug Administration (FDA)
Pfizer Consumer Healthcare Issues Voluntary Recall of One Lot of ThermaCare HeatWraps Menstrual Product, U.S. Food & Drug Administration (FDA)
FDA Warns three companies to stop making unproven claims on mouth rinses, U.S. Food & Drug Administration (FDA)
NIH and FDA announce awards to advance regulatory science, U.S. Food & Drug Administration (FDA)
ALLERGY ALERTS: Granola Thins, Butter Cup Cakes, Pork Ginger Sausage, FoodSafety.gov
FDA issues final rule on safety information during clinical trials, U.S. Food & Drug Administration (FDA)
HealthCare.gov on Facebook, HealthCare.gov
Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa), U.S. Food & Drug Administration (FDA)
FDA approves combination contraceptive containing a folate, U.S. Food & Drug Administration (FDA)
Similac Powder Infant Formulas: Recall-UPDATE: new searchable database and consumer update added, FDA MedWatch
FDA MedWatch - Octagam (Immune Globulin Intravenous (human)) 5% Liquid Preparation: Market Withdrawal - Risk of Thromboembolic Events, FDA MedWatch
FDA MedWatch - Epogen and Procrit (epoetin alfa): Recall - Particulate Matter in Vials, FDA MedWatch
FDA MedWatch - Electric Dental Handpieces and Electric Oral Bone-cutting Handpieces: Safety Investigation of Patient Burns, FDA MedWatch
Enforcement Report for September 22, 2010, U.S. Food & Drug Administration (FDA)
Similac Infant Formula: Get a Complete List of Products Recalled, FoodSafety.gov
CVM Updates - FDA to hold Public Workshop for Animal Health Industry on Release of Beta-Version of eSubmitter, an Electronic Submission Tool, U.S. Food & Drug Administration (FDA)
Red Lotus Bakery Issues Allergy Alert On Undeclared Eggs In "Butter Cup Cakes", U.S. Food & Drug Administration (FDA)
General Mills Issues Voluntary Class One Recall of One Day's Production of Nature Valley Dark Chocolate Flavor Granola Thins, U.S. Food & Drug Administration (FDA)
Six Months of the Affordable Care Act, HealthCare.gov
FDA MedWatch - Avandia (rosiglitazone): REMS - Risk of Cardiovascular Events, FDA MedWatch
FDA significantly restricts access to the diabetes drug Avandia, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Western Family Maple Nut Ice Cream, FoodSafety.gov
FDA MedWatch - Similac Powder Infant Formulas: Recall, FDA MedWatch
RECALL: Similac Powder Infant Formula, FoodSafety.gov
Deluxe Ice Cream Issues Allergy Alert on Undeclared Peanuts in Western Family Maple Nut Ice Cream, U.S. Food & Drug Administration (FDA)
Suzipoo Issues Allergy Alert on Undeclared Allergen in Lobster Poo, U.S. Food & Drug Administration (FDA)
Abbott Voluntarily Recalls Certain Similac® Brand Powder Infant Formulas That Did Not Meet Its Quality Standards, U.S. Food & Drug Administration (FDA)
ALLERGY ALERT: Garvi Gujarat brand Tam Tam (star noodle snack), FoodSafety.gov
House of Spices Issues Allergy Alert On Undeclared Peanuts in Garvi Gujarat Brand Tam Tam (Star Noodles) 10 oz., U.S. Food & Drug Administration (FDA)
NIH study models H1N1 flu spread, U.S. Dept. of Health & Human Services
FDA approves first oral drug to reduce MS relapses, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - CVM Annual Report for Fiscal Year 2009, U.S. Food & Drug Administration (FDA)
CVM Updates - FDA Announces Minor Use/Minor Species Grant Program Awards, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Aromatase Inhibitors in Products Marketed as Dietary Supplements: Recall, FDA MedWatch
ALLERGY ALERT: Oatmeal Raisin Cookies & Chocolate Chunk Cookies Sold at 7-eleven, FoodSafety.gov
Hallmark Fisheries Issues Recall of Crab Meat Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Dough Masters Inc. Issues Recall of Oatmeal Raisin Cookies and Chocolate Chunk Cookies Due to Undeclared Walnuts, U.S. Food & Drug Administration (FDA)
iForce Nutrition Issues a Voluntary Nationwide Recall of Reversitol a Product Marketed as a Dietary Supplement Containing ATD, U.S. Food & Drug Administration (FDA)
FDA Office of Women's Health Fall 2010 eUpdate, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Actos (pioglitazone): Ongoing Safety Review - Potential Increased Risk of Bladder Cancer, FDA MedWatch
FDA reviewing preliminary safety information on Actos (pioglitazone), U.S. Food & Drug Administration (FDA)
Advanced Muscle Science Issues a Voluntary Nationwide Recall of AROM-X Capsules, AROM-X UTT Liquid, AROM-XL Liquid, 4-AD Capsules and Decavol Capsules Marketed as a Dietary Supplements Containing ATD, U.S. Food & Drug Administration (FDA)
Fizogen Precision Technologies, Inc. Issues a Voluntary Nationwide Recall of OFF CYCLE II HARDCORE, a Product Marketed as a Dietary Supplement, U.S. Food & Drug Administration (FDA)
FDA , U. of Md., train Bangladeshis on aquaculture safety, U.S. Food & Drug Administration (FDA)
FDA hosts Middle East and North Africa food safety experts, U.S. Food & Drug Administration (FDA)
FDA approves devices for heart failure patients, U.S. Food & Drug Administration (FDA)
Twitter Chat at 3:30 pm ET Today: Food Safety for At-Risk People, FoodSafety.gov
G.E.T. Issues Vouluntary Recall of ArimaDex, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - September Green Book Update, U.S. Food & Drug Administration (FDA)
Kilosports Inc. Issues Voluntary Recall of Clomed, U.S. Food & Drug Administration (FDA)
Enforcement Report for September 15, 2010, U.S. Food & Drug Administration (FDA)
FDA MedWatch - BagEasy Manual Resuscitation Devices by Westmed, Inc.: Class 1 Recall, FDA MedWatch
August 2010 Drug Safety Labeling Changes: 24 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices, U.S. Food & Drug Administration (FDA)
Forest Pharmaceuticals agrees to guilty plea for violating FDA laws, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Valcyte (valganciclovir hydrochloride) Label Change: Possible overdose in pediatric patients, FDA MedWatch
FDA issues new dosing guide for children using Valcyte, U.S. Food & Drug Administration (FDA)
The Affordable Care Act & Behavioral Health, HealthCare.gov
FDA approves new drug for gout, U.S. Food & Drug Administration (FDA)
Webinar on Generic Drugs, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Availability of draft guidance re: development of antivirals for Chronic Hepatitis C, including coinfection with HIV, U.S. Food & Drug Administration (FDA)
FDA Hepatitis Update - Availability of draft Guidance: Chronic Hepatitis C Virus Infection: Developing Direct-Acting Antiviral Agents for Treatment, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recall: Libby & Kroger Corned Beef, Brushy Creek Beef Products, FoodSafety.gov
Influenza Vaccination Information for Health Care Workers, U.S. Dept. of Health & Human Services
How to Clean and Disinfect Schools to Help Slow the Spread of Flu, U.S. Dept. of Health & Human Services
Get information about high-risk groups, flu symptoms and emergency warning signs, and get CDC recommendations., U.S. Dept. of Health & Human Services
FDA MedWatch - Hospira Symbiq One-Channel and Two-Channel Infusers: Class I Recall - Potential for device to fail to detect air in line, FDA MedWatch
FDA MedWatch - Gadolinium-based Contrast Agents: Class Labeling Change - Risk of Nephrogenic Systemic Fibrosis, FDA MedWatch
FDA approves pediatric use of chemical poisoning treatment, U.S. Food & Drug Administration (FDA)
The September 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
FDA acts against 5 electronic cigarette distributors, U.S. Food & Drug Administration (FDA)
FDA: New warnings required on use of gadolinium-based contrast agents, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recall: Milk, FoodSafety.gov
Recall of Fluid Milk Products out of Midland Farms, Inc., U.S. Food & Drug Administration (FDA)
Enforcement Report for September 8, 2010, U.S. Food & Drug Administration (FDA)
How the Affordable Care Act Will Help Businesses and Unions Keep Early Retirees Covered, HealthCare.gov
FDA MedWatch - AngioSculpt "EX" PTCA Scoring Balloon Catheter by AngioScore, Inc.: Recall - Risk of Catheter Separation, FDA MedWatch
Undeclared Sulfites in "Rehmat" Brand Apricots, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Warning: Discard cheeses from Estrella Family Creamery, FoodSafety.gov
Cibo Vita issues Allergy Alert on Undeclared Sulfites in Mediterranean Mix of Woodpecker Brand, FoodSafety.gov
FoodSafety.gov Recall: Hartz Naturals Real Beef Treats for Dogs, FoodSafety.gov
FoodSafety.gov Recall: Egg Noodles & Wonton Skins, Possible Salmonella, FoodSafety.gov
Sparboe Farms Provides Clarification on its Voluntary Recall of Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
Real Taste Noodle Manufacture Recalls Egg Noodle Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA cautions consumers about Estrella Family Creamery cheeses, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Additional Materials for the AquAdvantage Salmon VMAC Meeting, U.S. Food & Drug Administration (FDA)
Good Taste Noodle MFG Recalls "Egg Noodles and Wonton Skins" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recalls: Whole Foods Recalls Raw Goat Milk Cheese, FoodSafety.gov
Whole Foods Market® Announces Recall of Morningland Dairy and Ozark Hills Farm Cheese, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentiative approval of lamivudine, nevirapine, and stavudine fixed dose combination tablets, 150 mg/200 mg/30 mg, U.S. Food & Drug Administration (FDA)
- <Possible follow-ups>
- HIV/AIDS Update - Tentiative approval of lamivudine, nevirapine, and stavudine fixed dose combination tablets, 150 mg/200 mg/30 mg, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recall: Cooked Shredded Pork Skin Products, FoodSafety.gov
FoodSafety.gov Recall Expanded: Queso Fresco and Requeson (Ricotta), FoodSafety.gov
Enforcement Report for September 1, 2010, U.S. Food & Drug Administration (FDA)
What do consumers need to know about the recall of shell eggs?, U.S. Food & Drug Administration (FDA)
Azteca Linda Corp. Expands Recall of Queso Fresco Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - P&G Voluntarily Recalls a Small Amount of Dry Cat Food, U.S. Food & Drug Administration (FDA)
P&G Voluntarily Recalls a Small Amount of Dry Cat Food, U.S. Food & Drug Administration (FDA)
FoodSafety.gov News Update, FoodSafety.gov
- <Possible follow-ups>
- FoodSafety.gov News Update, FoodSafety.gov
FoodSafety.gov Recall: Iams Cat Food Recalled from Stores in Loveland, Colorado, FoodSafety.gov
QUESERIA CHIPILO INC. Recalls Cheese Products because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA MedWatch - Tygacil (tigecycline): Label Change - Increased Mortality Risk, FDA MedWatch
FoodSafety.gov Allergy Alert: Peanuts in "Mixed Nuts Fancy, No Peanuts", FoodSafety.gov
FoodSafety.gov Recall: Morningland Dairy & Ozark Hills Farm cheeses, FoodSafety.gov
The September 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - new guidances available, U.S. Food & Drug Administration (FDA)
Torn & Glasser Issues Allergy Alert on Undeclared Peanuts Fancy, No Peanuts, U.S. Food & Drug Administration (FDA)
FDA seeks court order against Michigan dairy, U.S. Food & Drug Administration (FDA)
Paleta California Co. Announces Voluntary Recall of Frozen Mamey Paletas Because of Potential Contamination with Salmonella Typhi, U.S. Food & Drug Administration (FDA)
Morningland Dairy Conducting Nationwide Voluntary Recall of All Cheese Labeled as Morningland Dairy & Ozark Hills Farm Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FDA launches new organizational performance management system, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Green Book August 2010 Update, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recalls: "Fruiti Pops" Mamey Frozen Fruit Bars and Queseria Chipilo Cheese Products, FoodSafety.gov
P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recall: Ground Beef Distributed to BJ's Wholesale Club, FoodSafety.gov
Sparboe Farms Initiated Voluntary Recall Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
Fruiti Pops, Inc. Recalls "Fruiti Pops" Brand Mamey Frozen Fruit Bars Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
Queseria Chipilo Recalls Cheese Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Cal-Maine Foods, Inc. Clarifies Previous Statement on Nationwide Shell Egg Recall, U.S. Food & Drug Administration (FDA)
Estimating Seasonal Influenza-Associated Deaths in the U.S: CDC Study Confirms Variability of Flu, U.S. Dept. of Health & Human Services
FDA MedWatch - Huber Needles: Recall - Risk of Coring, FDA MedWatch
FDA MedWatch - Fingerstick Devices to Obtain Blood Specimens: Initial Communication - Risk of Transmitting Bloodborne Pathogens, FDA MedWatch
Enforcement Report for August 25, 2010, U.S. Food & Drug Administration (FDA)
Trafficanda Egg Ranch Initiates Voluntary Recall of Medium, Large, X Large, & Jumbo AA Cartons; 5 Dozen Medium Over Wrap & 20 Count Over Wrap, Fresh Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Cardenas Market Brand Label Included in Wright County Egg Recall, U.S. Food & Drug Administration (FDA)
FDA Warns Consumers to Avoid TimeOut Capsules, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recalls: Queso Fresco and Queso Hebra, FoodSafety.gov
Azteca Linda Corp. Recalls Queso Fresco and Queso Hebra because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Veterinary Medicine Advisory Committee Meeting Announcement, U.S. Food & Drug Administration (FDA)
Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed as a Dietary Supplement - 08/24/10, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Alert: Updated List of Recalled Egg Brands, FoodSafety.gov
The Power of Information at Your Fingertips, HealthCare.gov
FDA MedWatch - Mr. Magic Male Enhancer: Undeclared Drug Ingredient, FDA MedWatch
FDA releases guidance on federal menu labeling requirements, U.S. Food & Drug Administration (FDA)
FDA Warns of Possible Dangers from Portable Foot-Tanning Device, U.S. Food & Drug Administration (FDA)
Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter, U.S. Food & Drug Administration (FDA)
Moark, LLC, of Fontana, California, Recalls Shell Eggs Supplied From Hillandale Farms of Iowa Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Update: NuCal Foods Conducts Recall of Shell Eggs Supplied from Hillandale Farms of Iowa Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Recalls: 380,000 lbs of Deli Meat Products, Possible Listeria, FoodSafety.gov
FDA MedWatch - INOMAX DS Drug-Delivery System: Class I Recall - Risk of Interruption of Drug Flow, FDA MedWatch
NY Fish Inc Issues an alert on uneviscerated fish, U.S. Food & Drug Administration (FDA)
Study: Presence of murine leukemia virus found in CFS Patients, others, U.S. Food & Drug Administration (FDA)
NIH Office of Research on Women's Health - 20th Anniversary Celebration, U.S. Food & Drug Administration (FDA)
Luberski Inc. Initiates Voluntary Recall of Large Fresh Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
HIV/AIDS Update - Tentative approval of generic atazanavir sulfate capsules, 300 mg, U.S. Food & Drug Administration (FDA)
Milton's Baking Voluntarily Recalls 24 oz. Multi-Grain Bread in Three States For Undeclared Milk in Some Loaves, U.S. Food & Drug Administration (FDA)
GloryBee Foods Recalls Whole Raw Pistachio and Whole Raw Pistachio Kernels Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Austinuts Wholesale, Inc. Announces Voluntary Recall of Pistachio Kernel Products, U.S. Food & Drug Administration (FDA)
Review Calls for New Federal Approach to Medical Countermeasures, U.S. Dept. of Health & Human Services
Salmonella in Alfalfa Sprouts, U.S. Food & Drug Administration (FDA)
FoodSafety.gov Alert: URGENT Nationwide Frozen Mamey Fruit Pulp Recall, FoodSafety.gov
Hillandale Farms of Iowa Conducts Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
Urgent Nationwide Frozen Mamey Fruit Products Recall, U.S. Food & Drug Administration (FDA)
Stalevo(carbidopa/levodopa and entacapone): Ongoing Safety Review: Possible increased cardiovascular risk, FDA MedWatch
FoodSafety.gov Alert: URGENT Nationwide Egg Recall, FoodSafety.gov
FoodSafety.gov Recalls: "La Nuestra" Frozen Mamey Pulp, FoodSafety.gov
Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Frozen Mamey Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
Urgent Nationwide Egg Recall, U.S. Food & Drug Administration (FDA)
Update of CVM's What's New - Updated Minor Use/Minor Species Designations List, U.S. Food & Drug Administration (FDA)
COUNTRY Eggs, Inc. Initiates Voluntary Recall of Large AA Loose 15 dozen Fresh Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
U.S. Marshals seize food from rodent-infested Ga. warehouse, U.S. Food & Drug Administration (FDA)

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