FDA News
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- FDA MedWatch - January/February 2009 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 7, 2009
- From: U.S. Food & Drug Administration (FDA)
- Celeste Industries Corporation Recalls All Lots of simplySmart Remove Make Up Remover (January 5)
- From: U.S. Food & Drug Administration (FDA)
- National Brands Inc. Issues a Nationwide Recall of Topaz brand Wafer Rolls Because of Possible Health Risks (December 19)
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Class I Recall of Ophthalmic Surgical Device
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Class I Recall of Ophthalmic Surgical Device
- From: U.S. Food & Drug Administration (FDA)
- FDA Prevents Two Dairies from Adulterating Animal Drugs and Food
- From: U.S. Food & Drug Administration (FDA)
- Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23)
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Innohep (tinzaparin sodium) Dear Healthcare Professional Letter issued re: increased risk of death in renal impaired elderly
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 31, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves First Nucleic Acid Test to Screen for Additional Types of HIV in Donated Blood and Tissue
- From: U.S. Food & Drug Administration (FDA)
- Tainted Weight Loss Pills Flagged as Health Risks
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Drug for Patients with Advanced Prostate Cancer
- From: U.S. Food & Drug Administration (FDA)
- KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Stryker Custom Cranial Implant Kits: Class 1 recall due to lack of assurance of sterility and risk on infection
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves First Imaging Agent to Enhance Scans of Blood Flow
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Hydromorphone tablets [ETHEX] recalled due to oversided tablets and potential for over dosage
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 24, 2008
- From: U.S. Food & Drug Administration (FDA)
- Caution to Dog Owners About Chicken Jerky Products
- From: U.S. Food & Drug Administration (FDA)
- ETHEX Corporation Initiated Nationwide Voluntary Recall of a Single Lot of Hydromorphone HCl 2 mg Tablets Due to Potential for Oversized Tablet (December 23)
- From: U.S. Food & Drug Administration (FDA)
- KV Pharmaceutical Voluntarily Suspends All Shipments of its Approved Tablet-form Drugs (December 23)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Weight Loss Pills contain undeclared, active pharmaceutical ingredients that may put consumers' health at risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers About Tainted Weight Loss Pills (December 22)
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers About Tainted Weight Loss Pills
- From: U.S. Food & Drug Administration (FDA)
- FDA Obtains Injunction to Stop Production of Illegally Medicated Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- Dorsey Marketing Inc. Voluntarily Recalls Three G and J Gourmet Market Cocoa Products: 120126, 120129, 120144 (December 19)
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Gleevec to Prevent Recurrence of Rare Gastrointestinal Cancer
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - SunMed Greenline/D MacIntosh No. 3 Laryngoscope Blades recalled due to potential to break during use
- From: U.S. Food & Drug Administration (FDA)
- Preliminary Animal Health Notification - Chicken Jerky Products for Dogs
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - October 2008 Drug Safety Labeling Changes for 61 Drugs Now Available on Web
- From: U.S. Food & Drug Administration (FDA)
- Interfood Shareholding Company Issues a Nationwide recall of Wonderfarm Brand Biscuits Because of Possible Health Risk (December 9)
- From: U.S. Food & Drug Administration (FDA)
- Historic Building One Dedicated at FDA?s White Oak Federal Research Center
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Drug that Boosts Stem Cell Yield for Bone Marrow Transplants
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces New Recommendations on Evaluating Cardiovascular Risk in Drugs Intended to Treat Type 2 Diabetes
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 17, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Requires Warnings about Risk of Suicidal Thoughts and Behavior for Antiepileptic Medications
- From: U.S. Food & Drug Administration (FDA)
- Botulism Risk From Ungutted, Salt-Cured Alewives Fish
- From: U.S. Food & Drug Administration (FDA)
- Prescription Drug Leaflets Need Improvement
- From: U.S. Food & Drug Administration (FDA)
- Study Finds Much of Private-Sector Consumer Medication Information Not Consistently Useful
- From: U.S. Food & Drug Administration (FDA)
- Kidney Risk Spurs Warning on Bowel Cleansers
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Class I Recalls of Two Unapproved Devices (December 15)
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Class I Recalls of Two Unapproved Devices
- From: U.S. Food & Drug Administration (FDA)
- Kashi Company Issues Allergy Alert on Undeclared Milk in Kashi GOLEAN® Powder Chocolate Energy Shake Mix (December 13)
- From: U.S. Food & Drug Administration (FDA)
- Urgent: Food Product Recall Re: Imitation Cream Cheese and Low Protein Peanot Butter(December 11)
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers and Retailers of Botulism Risk from Ungutted, Salt-Cured Alewives (Gaspereaux) Fish (December 12)
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers and Retailers of Botulism Risk from Ungutted, Salt-Cured Alewives (Gaspereaux) Fish
- From: U.S. Food & Drug Administration (FDA)
- Get Set for Winter Illness Season
- From: U.S. Food & Drug Administration (FDA)
- Some Medications and Driving Don't Mix
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Oral Sodium Phosphate (OSP) Products for Bowel Cleansing: reports of acute phosphate nephropathy, Boxed Warning to be added to labeling
- From: U.S. Food & Drug Administration (FDA)
- FDA Requires New Safety Measures for Oral Sodium Phosphate Products to Reduce Risk of Acute Kidney Injury
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Gravity Compensating Accessory by Integra NeuroSciences: recalled because devices may leak cerebrospinal fluid
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Healon D Ophthalmic Viscosurgical Device: recall due to syringes with endotoxin levels above the required limit
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 10, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Education Program Wins Award
- From: U.S. Food & Drug Administration (FDA)
- FDA Beyond Our Borders
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Permanent Injunction Against Wilderness Family Naturals LLC
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - 20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP: Recall of one lot due to possible incorrect bar code for 5% Dextrose Injection, USP.
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5 Percent Dextrose and 0.45 Percent Sodium Chloride Injection, USP Due to Incorrect Bar Code Label (December 8)
- From: U.S. Food & Drug Administration (FDA)
- Balanced Health Products, Inc. Expands Voluntary Urgent Nationwide Recall of Starcaps Dietary Supplement Capsules Found to Contain an Undeclared Drug Ingredient (December 8)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch-Terumo Cardiovascular Systems Tenderflow Pediatric Arterial Cannulae- Recalled due to reports of difficulty retracting the introducer from the cannula
- From: U.S. Food & Drug Administration (FDA)
- Terumo Cardiovascular Systems Issues Urgent, Nationwide/Worldwide Recall of Pediatric Arterial Cannulae (December 8)
- From: U.S. Food & Drug Administration (FDA)
- Louisiana Fish Fry Products Issues Nationwide Allergy Alert on Undeclared Buttermilk in Chicken and Fish Bake Seasoned Coating Mix (December 5)
- From: U.S. Food & Drug Administration (FDA)
- Walgreens Recalls 173 Teddy Bears With Chocolate Bars Sold Since Late September 2008 (December 5)
- From: U.S. Food & Drug Administration (FDA)
- Mom's Food Products, Inc. Issues Allergy Alert On Undeclared Eggs In Pimento Spread Sandwiches (December 2)
- From: U.S. Food & Drug Administration (FDA)
- Limited Recall of LAND O LAKES Sheep Balancer B136 (December 4)
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 03, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA, EPA and USDA Conclude That Accidental Release of Genetically Engineered Cotton Poses No Safety Risk to Humans or Animals
- From: U.S. Food & Drug Administration (FDA)
- Drug Information Update- FDA Teams With WebMD For New Online Consumer Health Information
- From: U.S. Food & Drug Administration (FDA)
- FDA Announces Participants of Pilot Program for Third-Party Certification of Imported Aquacultured Shrimp
- From: U.S. Food & Drug Administration (FDA)
- FDA Partners With WebMD to Better Serve Consumers
- From: U.S. Food & Drug Administration (FDA)
- FDA Teams With WebMD For New Online Consumer Health Information
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Innohep (tinzaparin): Clinical study stopped early because of interim finding of increased all-cause mortality in patients who received drug
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - The December 2008 Patient Safety News Is Now Available...
- From: U.S. Food & Drug Administration (FDA)
- FDA Reports Significant Progress in Protecting the Food Supply
- From: U.S. Food & Drug Administration (FDA)
- FDA Acts to Reduce Risk of Salmonella Infections
- From: U.S. Food & Drug Administration (FDA)
- Avoiding Drug Interactions
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 26, 2008
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Zhen De Shou Fat Loss Capsules recalled due to undeclared drug, sibutramine which may cause significant increase in blood pressure
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Starcaps Dietary Supplement Capsules - Recall due to undeclared drug, Bumetanide, resulting in drug interactions, hypotension
- From: U.S. Food & Drug Administration (FDA)
- Balanced Health Products, Inc. Conducts Voluntary Urgent Nationwide Recall of Starcaps Dietary Supplement Capsules Found to Contain an Undeclared Drug Ingredient (November 24)
- From: U.S. Food & Drug Administration (FDA)
- Fashion Sanctuary Issues a Voluntary Nationwide Recall of All Lots of Zhen De Shou Fat Loss Capsules Found to Contain an Undeclared Drug Ingredient (November 23)
- From: U.S. Food & Drug Administration (FDA)
- Stop and Shop Recalls Butternut Squash in Prepared Turkey and Ham Dinner (November 24)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Phenytoin and Fosphenytoin Sodium associated with potential increased risk of serious skin reactions
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves New Drug to Alleviate Moderate to Severe Pain
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Animas Insulin Pumps: Battery Caps - Class 1 recall due to inadvertent device resetting, risk of hyperglycemia
- From: U.S. Food & Drug Administration (FDA)
- PANOS Brands Recalls Vegan Rella Cheddar Block (November 21)
- From: U.S. Food & Drug Administration (FDA)
- FDA Acts to Avoid Shortage and Strengthen the Safety of Sucraid
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Food Markets, Inc. Issues Voluntary Recall on Wegmans Italian Classics Seasoned Tomato Sauce (November 20)
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves New Drug to Treat Severe Form of Epilepsy
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 19, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch: Benzoyl Peroxide Acne Cream 10%: Product Recalled Because Samples Contained Burkholderia Cepacia Bacteria
- From: U.S. Food & Drug Administration (FDA)
- Beware of Extortion Scam by FDA Impersonators
- From: U.S. Food & Drug Administration (FDA)
- Seattle's Favorite Gourmet Cookies and Dessert Co Issues Nationwide Allergy Alert on Undeclared Milk in Muffin Tops (November 14)
- From: U.S. Food & Drug Administration (FDA)
- CSI USA, Inc. Issues Voluntary National Recall of Topical Acne Cream (November 13)
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 12, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Public of Extortion Scam by FDA Impersonators
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Bisphosphonates-Update To The Early Communication Issued Regarding Atrial Fibrillation With Bisphosphonates
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- FDA MedWatch- Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas)- Product Recalled Due To Possible Metal Fragments In The Bottle
- From: U.S. Food & Drug Administration (FDA)
- Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments (November 7)
- From: U.S. Food & Drug Administration (FDA)
- Amy's Kitchen Inc. Issues Allergy Alert and Voluntary National Recall due to Possible Undeclared Milk in Tofu Scramble in a Pocket Sandwich; Lot Code H148 (November 7)
- From: U.S. Food & Drug Administration (FDA)
- Nestle Withdraws Nestle Farinha Lactea Cereal in the United States (November 3)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- FDA MedWatch- Propafenone HCl, Isosorbide Mononitrate Extended Release, Morphine Sulfate Immediate and Extended Release, Dextroamphetamine Sulfate- Products Recalled Due To The Potential For Oversized Tablets
- From: U.S. Food & Drug Administration (FDA)
- ETHEX Corporation Initiated Nationwide Voluntary Recalls of Specific Lots of Five Generic Products Due to the Potential for Oversized Tablets (November 7)
- From: U.S. Food & Drug Administration (FDA)
- Nestle USA Voluntarily Recalls Two Production Codes of Nestle Nesquik Strawberry Powder (November 7)
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - WalMart "ReliOn" insulin syringe recall due to potential for serious overdose
- From: U.S. Food & Drug Administration (FDA)
- FDA Seizes Contaminated Heparin from a Cincinnati Manufacturer
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 5, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes (November 5)
- From: U.S. Food & Drug Administration (FDA)
- FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes (November 5)
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Tips for Healthy Holidays
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - September 2008 Drug Safety-Related Labeling Changes for 36 Drugs Now Available on Web
- From: U.S. Food & Drug Administration (FDA)
- General Mills Issues Voluntary Class One Recall Involving One Day's Production of Progresso Hearty Tomato Soup (October 31)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator- Class I Recall Because Of Unsupported Claims
- From: U.S. Food & Drug Administration (FDA)
- Everlasting Distributors Inc. Issues a Nationwide Recall of Fresh and Crispy Jacobina Biscuits Because of Possible Health Risks (October 29)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - The November 2008 Patient Safety News Is Now Available...
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Toviaz, a New Drug to Treat Overactive Bladder
- From: U.S. Food & Drug Administration (FDA)
- HHS/FDA Grants Tentative Approval for 75th Generic Anti-Retroviral Drug as Part of President's Emergency Plan for AIDS Relief
- From: U.S. Food & Drug Administration (FDA)
- Mexican Vanilla With Coumarin: No Bargain
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 29, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Statement on Release of Bisphenol A (BPA) Subcommittee Report
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Thoratec HeartMate II Left Ventricular Assist System- Device Correction: Wear And Fatigue Of The Percutaneous Lead Connecting The Blood Pump With The System Controller May Cause Serious Injury Or Death
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Bayer About Two Unapproved Aspirin Products
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Warning Letters to Bayer HealthCare for Illegally Marketing Two Unapproved Drugs
- From: U.S. Food & Drug Administration (FDA)
- Mars Petcare US Issues Voluntary Recall of a Limited Number of Bags of SPECIAL KITTY Gourmet Sold at Wal-Mart locations in Fifteen States due to Potential Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Thoratec Corporation Issues Worldwide Medical Device Correction of HeartMate II Left Ventricular Assist System (October 24)
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Lung Valve to Control Some Air Leaks after Surgery
- From: U.S. Food & Drug Administration (FDA)
- Portland Shellfish Co. Inc, Recalls Claw Island Brand Lobster Claw and Knuckle Meat Because of Possible Health Risk (October 21)
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 22, 2008
- From: U.S. Food & Drug Administration (FDA)
- Nonna's Real Italiana Cuccine Issues an Allergy Alert on Undeclared Milk, Soy, and Wheat in Stuffed Artichokes (October 22)
- From: U.S. Food & Drug Administration (FDA)
- Harry and David Issues Nationwide Allergy Alert on Undeclared Pecans in Harry and David Moose Munch Confection, Milk Chocolate Gingerbread (October 22)
- From: U.S. Food & Drug Administration (FDA)
- Using Over-the-Counter Cough and Cold Products in Children
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch: Transvaginal Placement of Surgical Mesh- Serious Complications Associated With Transvaginal Placement Of Surgical Mesh In Repair of Pelvic Organ Prolapse And Stress Urinary Incontinence
- From: U.S. Food & Drug Administration (FDA)
- The Hartz Mountain Corporation Voluntarily Recalls One Specific Lot of Nationwide Chicken-Basted Rawhide Chips Because of Possible Health Risk (October 20)
- From: U.S. Food & Drug Administration (FDA)
- Safety Concerns and Labeling Changes for Psoriasis Drug Raptiva
- From: U.S. Food & Drug Administration (FDA)
- Lotte USA, Inc. Initiates Nationwide Recall of Koala's March Creme filled Cookies
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Raptiva (efalizumab): Boxed Warning describes risk for life-threatening infections
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Updated Labeling for Psoriasis Drug Raptiva
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Dextroamphetamine Sulfate 5mg Tablets- Drug Recall Due To The Potential For Oversized Tablets
- From: U.S. Food & Drug Administration (FDA)
- Use Caution With Ayurvedic Products
- From: U.S. Food & Drug Administration (FDA)
- Improper Use of Decorative Contacts May Haunt You
- From: U.S. Food & Drug Administration (FDA)
- ETHEX Corporation Voluntarily Recalls Three Lots of Dextroamphetamine Sulfate 5mg Tablets Due to the Potential for Oversized Tablets (October 15)
- From: U.S. Food & Drug Administration (FDA)
- FDA Creates Web Page with Drug Safety Information for Patients, Health Care Professionals
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 15, 2008
- From: U.S. Food & Drug Administration (FDA)
- JFC International, Inc. Issues Allergy Alert on Undeclared Sulfite in "Kyosai Sengiri Daikon" Dried Radish (October 10)
- From: U.S. Food & Drug Administration (FDA)
- Barry Callebaut USA LLC Issues Allergen Alert on Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips (October 10)
- From: U.S. Food & Drug Administration (FDA)
- HUA XIA Food Trade USA, Inc. Recalls YILI Brand Sour Milk Drink and YILI Brand Pure Milk Drink, Because of Possible Health Risk (October 10)
- From: U.S. Food & Drug Administration (FDA)
- FDA Licenses for Marketing New Therapy for Rare Genetic Disease
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Rapaflo for the Treatment of Symptoms Due to an Enlarged Prostate Gland
- From: U.S. Food & Drug Administration (FDA)
- FDA Launches Food Defense Awareness Training Kit for Employees in the Food Industry
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 8, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Licenses Drug to Prevent Joint Damage in Children with Hemophilia A
- From: U.S. Food & Drug Administration (FDA)
- Russell Stover Candies, Inc. Issues Hazelnut Allergy Alert for the 2 7/8 Oz Size Of Private Reserve Assorted Chocolates (October 9)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- OTC Cough and Cold Medicines- Product Labels Being Modified To State " Do Not Use" In Children Under 4 Years Of Age
- From: U.S. Food & Drug Administration (FDA)
- Drug Information Update- FDA Statement Following CHPA's Announcement on Nonprescription Over-the-Counter Cough and Cold Medicines in Children
- From: U.S. Food & Drug Administration (FDA)
- Recalls and Melamine Contamination
- From: U.S. Food & Drug Administration (FDA)
- Consumer Alert: Undeclared Sulfites in Shad Raisins (October 6)
- From: U.S. Food & Drug Administration (FDA)
- Arnold Foods Company, Inc. Issues Allergy Alert on Undeclared Nuts in Brownberry Whole Grains Bread 100 Percent Whole Wheat (October 8)
- From: U.S. Food & Drug Administration (FDA)
- Consumer Alert: Possible Botulism Contamination in Frozen Salted Croaker (October 6)
- From: U.S. Food & Drug Administration (FDA)
- FDA Statement Following CHPA's Announcement on Nonprescription Over-the-Counter Cough and Cold Medicines in Children
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Use of Temporary Pump to Assist Heart's Right Side
- From: U.S. Food & Drug Administration (FDA)
- MedWatch - Tiotropium (Spiriva): updated information on risk of stroke and reports of cardiovascular adverse outcomes
- From: U.S. Food & Drug Administration (FDA)
- FDA and PATH Malaria Vaccine Initiative Announce Research Collaboration
- From: U.S. Food & Drug Administration (FDA)
- FDA Detects Melamine Contamination in Flavored Drink
- From: U.S. Food & Drug Administration (FDA)
- FDA Detects Melamine Contamination in Flavored Drink
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - CVM Announces Availability of Revised 356v Form
- From: U.S. Food & Drug Administration (FDA)
- McCormick and Company Has Recalled McCormick Enchilada Sauce Mix Due To Unlabeled Milk Ingredients (September 30)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Nebion HLX-8 Magnetic Resonance Device: Device Not Approved By FDA
- From: U.S. Food & Drug Administration (FDA)
- Tristar Food Wholesale Co Inc. Issues a Nationwide recall of Blue Cat Flavor Drink Because of Possible Health Risk (October 3)
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Interim Safety and Risk Assessment of Melamine and Melamine-related Compounds in Food
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- Medtronic Neuromodulation INDURA One-Piece Intrathecal Catheters, Sutureless Pump Connector Revision Kit, and Intrathecal Catheter Pump Segment Revision Kit- Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- Lion Pavilion Issues Alert on Undeclared Sulfites in Yulanpian Brand Dried Slices of Tender Bamboo Shoots (September 26)
- From: U.S. Food & Drug Administration (FDA)
- Mr. Brown 3-In-1 and and 2-In-1 Powdered Packets in Bag Coffee Mixes Due To Health Risk (October 1)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - The October 2008 FDA Patient Safety News Video is now available...
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 1, 2008
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Launches New Public-access Database of Animal Drug Approvals
- From: U.S. Food & Drug Administration (FDA)
- FDA Awards $5.2 Million in Grants to Further Food and Feed Safety
- From: U.S. Food & Drug Administration (FDA)
- FDA Awards up to $2.5 Billion to Modernize Information Technology over Ten Years
- From: U.S. Food & Drug Administration (FDA)
- NY Fish Inc. Recalls Imperial-European Style Smoked Salmon Because of Possible Health Risk (September 26)
- From: U.S. Food & Drug Administration (FDA)
- Keeping Watch Over Direct-to-Consumer Ads
- From: U.S. Food & Drug Administration (FDA)
- Is It Really FDA Approved?
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Statin drugs and risk of amyotrophic lateral sclerosis (ALS)
- From: U.S. Food & Drug Administration (FDA)
- FDA Analysis Shows Cholesterol Lowering Medications Do Not Increase the Risk of Lou Gehrig's Disease
- From: U.S. Food & Drug Administration (FDA)
- Addressing Questions About Gardasil
- From: U.S. Food & Drug Administration (FDA)
- QFCO, Inc. Recalls White Rabbit Candy Because of Possible Health Risk (September 26)
- From: U.S. Food & Drug Administration (FDA)
- Vaccines Stand Ready for Flu Season
- From: U.S. Food & Drug Administration (FDA)
- FDA Updates Health Information Advisory on Melamine Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA Updates Health Information Advisory on Melamine Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Epoetin alfa- Preliminary Safety Findings Show More Deaths In Patients Given Epoetin-alpha Versus Placebo
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 24, 2008
- From: U.S. Food & Drug Administration (FDA)
- CaJohns Fiery Foods Company Recalls HDH Grillin' Sauce (September 24)
- From: U.S. Food & Drug Administration (FDA)
- Mom's Food Products, Inc. Issues Allergy Alert On Undeclared Eggs in Sandwiches and Potato Salad (September 23)
- From: U.S. Food & Drug Administration (FDA)
- Fineland Corp Issues Alert on Undeclared Sulfites in Ying Feng Foodstuffs Brand Pumpkin Seeds (September 23)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Ammonul (sodium phenylacetate and sodium benzoate) Injection 10%/10% - Particulate matter detected in product
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Tarceva (erlotinib) - Cases of hepatic failure and hepatorenal syndrome, including fatalities, have been reported during use of Tarceva
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Companies to Stop Marketing Unapproved Ophthalmic Balanced Salt Solution Drug Products and Topical Drug Products Containing Papain
- From: U.S. Food & Drug Administration (FDA)
- FDA Updates Health Information Advisory on Melamine Contamination
- From: U.S. Food & Drug Administration (FDA)
- Derringer Foodservices Issues Allergy Alert on Albacore Tuna Salad Hoagie (September 17)
- From: U.S. Food & Drug Administration (FDA)
- K-Fat Inc. Issues Alert On Undeclared Sulfites In "Mut Gung Sweetened Ginger" (September 18)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch- FDA Drug Safety Newsletter- Summer 2008 Edition Available For Healthcare Professionals And The Medical Community
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Phosphocol P 32- Risk Of Leukemia Associated With Off-Label Intra-articular Use In Children
- From: U.S. Food & Drug Administration (FDA)
- Draft Guidance on Genetically Engineered Animals
- From: U.S. Food & Drug Administration (FDA)
- FDA Proposes Label Requirements for Refused Imported Foods
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 17, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Draft Guidance on Regulating Genetically Engineered Animals
- From: U.S. Food & Drug Administration (FDA)
- Bimbo Bakeries USA Issues an Allergy Alert on Undeclared Tree Nuts in Oroweat 100 Percent Whole Wheat Bread Packaging (September 16)
- From: U.S. Food & Drug Administration (FDA)
- Drug Information Update- FDA Issues Warning Letters to Ranbaxy Laboratories Ltd., and an Import Alert for Drugs from Two Ranbaxy Plants in India
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Warning Letters to Ranbaxy Laboratories Ltd., and an Import Alert for Drugs from Two Ranbaxy Plants in India
- From: U.S. Food & Drug Administration (FDA)
- In-Body Pediatric Devices Pose Unique Challenges
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - August 2008 Drug Safety-Related Labeling Changes for 41 Drugs Now Available on Web
- From: U.S. Food & Drug Administration (FDA)
- Ralston Foods Issues Allergy Alert For Undeclared Milk Ingredients In Western Family Variety Pack Instant Oatmeal (September 15)
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert on Undeclared Dairy in Margaritaville Island Lime Tortilla Chips (September 12)
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Expands Dates of Bagel Recall and Includes Additional Bakery Products (September 11)
- From: U.S. Food & Drug Administration (FDA)
- FDA Requires Stronger Fungal Infection Warning for TNF Blockers
- From: U.S. Food & Drug Administration (FDA)
- Health Information Advisory on Infant Formula
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for August 18, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for August 11, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for July 28, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for July 15, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for July 7, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for June 9, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for June 2, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for May 27, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for May 19, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for May 12, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for May 5, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for April 28, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for April 7, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for March 31, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for March 18, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for March 10, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for March 3, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for February 25, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for February 19, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for February 11, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for February 4, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for January 28, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for January 22, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for January 14, 2008
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for January 7, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for December 18, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for December 10, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for December 3, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for November 26, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for November 19, 2007
- From: U.S. Food & Drug Administration (FDA)
- FDA News Digest for November 13, 2007
- Notice to FDA News Digest subscribers
- FDA News Digest for November 5, 2007
- FDA News Digest for October 9, 2007
- FDA News Digest for October 1, 2007
- FDA News Digest for September 24, 2007
- FDA News Digest for September 17, 2007
- FDA News Digest for September 10, 2007
- FDA News Digest for September 4, 2007 (resend due to non-functioning link)
- FDA News Digest for August 27, 2007
- FDA News Digest for August 20, 2007
- FDA News Digest for August 13, 2007
- FDA News Digest for August 6, 2007
- FDA News Digest for July 30, 2007
- FDA News Digest for July 23, 2007
- FDA News Digest for July 16, 2007
- FDA News Digest for July 9, 2007
- FDA News Digest for July 2, 2007
- FDA News Digest for June 25, 2007
- FDA News Digest for June 18, 2007
- FDA News Digest for June 11, 2007
- FDA News Digest for June 4, 2007
- FDA News Digest for May 29, 2007
- FDA News Digest for May 21, 2007
- FDA News Digest for May 14, 2007
- FDA News Digest for May 7, 2007
- FDA News Digest for April 30, 2007
- FDA News Digest for April 23, 2007
- FDA News Digest for April 16, 2007
- FDA News Digest for April 9, 2007
- FDA News Digest for April 2, 2007
- This week's News Digest draft
- FDA News Digest for March 19, 2007
- FDA News Digest for March 12, 2007
- FDA News Digest for March 5, 2007
- FDA News Digest for February 26, 2007
- FDA News Digest for February 20, 2007
- FDA News Digest for February 12, 2007
- FDA News Digest for February 5, 2007
- FDA News Digest for January 29, 2007
- FDA News Digest for January 22, 2007
- FDA News Digest for January 16, 2007
- FDA News Digest for January 8, 2007
- FDA News Digest for January 3, 2007
- FDA News Digest for December 18, 2006
- FDA News Digest for December 11, 2006
- FDA News Digest for December 4, 2006
- FDA News Digest for November 27, 2006
- FDA News Digest for November 20, 2006
- FDA News Digest for November 13, 2006
- FDA News Digest for November 6, 2006
- FDA News Digest for October 30, 2006
- FDA News Digest for October 23, 2006
- FDA News Digest for October 16, 2006
- FDA News Digest for October 10, 2006
- FDA News Digest for October 2, 2006
- FDA News Digest for September 25, 2006
- FDA News Digest for September 18, 2006
- FDA News Digest for September 11, 2006
- FDA News Digest for September 5, 2006
- FDA News Digest for August 28, 2006
- FDA News Digest for August 21, 2006
- FDA News Digest for August 14, 2006
- FDA News Digest for August 7, 2006
- FDA News Digest for July 31, 2006
- FDA News Digest for July 24, 2006
- FDA News Digest for July 17, 2006
- FDA News Digest for July 10, 2006
- FDA News Digest for July 3, 2006
- FDA News Digest for June 26, 2006
- FDA News Digest for June 19, 2006
- FDA News Digest for June 12, 2006
- FDA News Digest for June 5, 2006
- FDA News Digest for May 30, 2006
- FDA News Digest for May 22, 2006
- FDA News Digest for May 15, 2006
- FDA News Digest for May 8, 2006
- FDA News Digest for May 1, 2006
- FDA News Digest for April 24, 2006
- FDA News Digest for April 17, 2006
- FDA News Digest for April 10, 2006
- FDA News Digest for April 3, 2006
- FDA News Digest for March 27, 2006
- FDA News Digest for March 20, 2006
- FDA News Digest for March 13, 2006
- FDA News Digest for March 6, 2006
- FDA News Digest for February 27, 2006
- FDA News Digest for February 21, 2006
- FDA News Digest for February 13, 2006
- FDA News Digest for February 6, 2006
- FDA News Digest for January 30, 2006
- FDA News Digest for January 23, 2006
- FDA News Digest for January 17, 2006
- FDA News Digest for January 9, 2006
- FDA News Digest for January 3, 2006
- FDA News Digest for December 19, 2005
- FDA News Digest for December 12, 2005
- FDA News Digest for December 5, 2005
- FDA News Digest for November 28, 2005
- FDA News Digest for November 21, 2005
- FDA News Digest for November 14, 2005
- FDA News Digest for November 7, 2005
- FDA News Digest for October 31, 2005
- FDA News Digest for October 24, 2005
- FDA News Digest for October 17, 2005
- FDA News Digest for October 11, 2005
- FDA News Digest for October 3, 2005
- FDA News Digest for September 26, 2005
- FDA News Digest for September 19, 2005
- FDA News Digest for September 12, 2005
- FDA News Digest for September 6, 2005
- FDA News Digest for August 29, 2005
- FDA News Digest for August 22, 2005
- FDA News Digest for August 15, 2005
- FDA News Digest for August 8, 2005
- FDA News Digest for August 1, 2005
- FDA News Digest for July 25, 2005
- FDA News Digest for July 18, 2005
- FDA News Digest for July 11, 2005
- FDA News Digest for July 5, 2005
- FDA News Digest for June 27, 2005
- FDA News Digest for June 20, 2005
- FDA News Digest for June 13, 2005
- FDA News Digest for June 6, 2005
- FDA News Digest for May 31, 2005
- FDA News Digest for May 23, 2005
- FDA News Digest for May 16, 2005
- FDA News Digest for May 9, 2005
- FDA News Digest for May 2, 2005
- FDA News Digest for April 25, 2005
- FDA News Digest for April 18, 2005
- FDA News Digest for April 11, 2005
- FDA News Digest for April 4, 2005
- FDA News Digest for March 28, 2005
- FDA News Digest for March 21, 2005
- FDA News Digest for March 14, 2005
- FDA News Digest for March 7, 2005
- FDA News Digest for February 28, 2005
- FDA News Digest for February 22, 2005
- FDA News Digest for February 14, 2005
- FDA News Digest for February 7, 2005
- FDA News Digest for January 31, 2005
- FDA News Digest for January 24, 2005
- FDA News Digest for January 10, 2005
- FDA News Digest for January 3, 2005
- FDA News Digest for December 20, 2004
- FDA News Digest for December 13, 2004
- FDA News Digest for December 6, 2004
- FDA News Digest for November 29, 2004
- FDA News Digest for November 22, 2004
- FDA News Digest for November 15, 2004
- FDA News Digest for November 8, 2004
- FDA News Digest for November 1, 2004
- FDA News Digest for October 25, 2004
- FDA News Digest for October 18, 2004
- FDA News Digest for October 12, 2004
- FDA News Digest for October 4, 2004
- FDA News Digest for September 27, 2004
- FDA News Digest for September 20, 2004
- FDA News Digest for September 13, 2004
- FDA News Digest for September 7, 2004
- FDA News Digest for August 30, 2004
- FDA News Digest for August 23, 2004
- FDA News Digest for August 16, 2004
- FDA News Digest for August 9, 2004
- FDA News Digest for August 2, 2004
- FDA News Digest for July 26, 2004
- FDA News Digest for July 19, 2004
- FDA News Digest for July 12, 2004
- FDA News Digest for July 6, 2004
- FDA News Digest for June 28, 2004
- FDA News Digest for June 21, 2004
- FDA News Digest for June 14, 2004
- FDA News Digest for June 7, 2004
- FDA News Digest for June 1, 2004
- FDA News Digest for May 3, 2004
- FDA News Digest for April 26, 2004
- FDA News Digest for April 19, 2004
- FDA News Digest for April 12, 2004
- FDA News Digest for April 5, 2004
- FDA News Digest for March 29, 2004
- FDA News Digest for March 22, 2004
- FDA News Digest for March 15, 2004
- FDA News Digest for March 8, 2004
- FDA News Digest for March 1, 2004
- FDA News Digest for February 23, 2004
- FDA News Digest for February 17, 2004
- FDA News Digest for February 9, 2004
- FDA News Digest for February 2, 2004
- FDA News Digest for January 26, 2004
- FDA News Digest for January 20, 2004
- FDA News Digest for January 12, 2004
- FDA News Digest for January 5, 2004
- FDA News Digest for December 22, 2003
- FDA News Digest for December 15, 2003
- FDA News Digest for December 8, 2003
- FDA News Digest for December 1, 2003
- FDA News Digest for November 24, 2003
- FDA News Digest for November 17, 2003
- FDA News Digest for November 10, 2003
- FDA News Digest for November 3, 2003
- FDA News Digest for October 27, 2003
- FDA News Digest for October 20, 2003
- FDA News Digest for October 14, 2003
- FDA News Digest for October 6, 2003
- FDA News Digest for September 29, 2003
- FDA News Digest for September 22, 2003
- FDA News Digest for September 15, 2003
- FDA News Digest for September 8, 2003
- FDA News Digest for September 2, 2003
- FDA News Digest for August 25, 2003
- FDA News Digest for August 18, 2003
- FDA News Digest for August 11, 2003
- FDA News Digest for August 4, 2003
- FDA News Digest for July 28, 2003
- FDA News Digest for July 21, 2003
- FDA News Digest for July 14, 2003
- FDA News Digest for July 7, 2003
- FDA News Digest for June 30, 2003
- FDA News Digest for June 23, 2003
- FDA News Digest for June 16, 2003
- FDA News Digest for June 9, 2003
- FDA News Digest for June 2, 2003
- FDA News Digest for May 27, 2003
- FDA News Digest for May 19, 2003
- FDA News Digest for May 12, 2003
- FDA News Digest for May 5, 2003
- FDA News Digest for April 28, 2003
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- FDA News Digest for April 14, 2003
- FDA News Digest for April 7, 2003
- FDA News Digest for March 24, 2003
- FDA News Digest for March 17, 2003
- FDA News Digest for March 10, 2003
- FDA News Digest for March 3, 2003
- FDA News Digest for February 24, 2003
- FDA News Digest for February 19, 2003
- FDA News Digest for February 10, 2003
- FDA News Digest for February 3, 2002
- FDA News Digest for January 27, 2003
- FDA News Digest for January 21, 2003
- FDA News Digest for January 13, 2003
- FDA News Digest for January 6, 2003
- FDA News Digest for December 23, 2002
- FDA News Digest for December 16, 2002
- FDA News Digest for December 9, 2002
- FDA News Digest for December 2, 2002
- FDA News Digest for November 25, 2002
- FDA News Digest for November 18, 2002
- FDA News Digest for November 12, 2002
- FDA News Digest for November 4, 2002
- FDA News Digest for October 28, 2002
- FDA News Digest for October 21, 2002
- FDA News Digest for October 15, 2002
- FDA News Digest for October 7, 2002
- FDA News Digest for September 23, 2002
- FDA News Digest for September 16, 2002
- FDA News Digest for September 9, 2002
- FDA News Digest for September 3, 2002
- FDA News Digest for August 26, 2002
- FDA News Digest for August 19, 2002
- FDA News Digest for August 12, 2002
- FDA News Digest - August 5, 2002
- FDA News Digest for July 29, 2002
- FDA News Digest for July 22, 2002
- FDA News Digest for July 15, 2002
- FDA News Digest for July 8, 2002
- FDA News Digest for July 1, 2002
- FDA News Digest for June 17, 2002
- FDA News Digest for June 10, 2002
- Note to Subscribers
- FDA News Digest for June 3, 2002
- FDA News Digest for May 28, 2002
- FDA News Digest for May 20, 2002
- FDA News Digest for May 13, 2002