FDA News

• Thread Index

• Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination
  • From: U.S. Dept. of Health & Human Services
• Cheese Recall and Allergy Alerts (Gelato, Custard Pie, Sausage)
  • From: U.S. Dept. of Health & Human Services
• Azteca Linda Corp. Recalls QUESO FRESCO and QUESO HEBRA Because of Possible Risk of Health
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• DOMEGA NY INTERNATIONAL CO., LTD Issues Allergy Alert on Undeclared Milk Powder in FUMA CUSTARD PIE
  • From: U.S. Food & Drug Administration (FDA)
• I Dolce Inc. Issues Allergy Alert on Undeclared Peanuts in "Gelato"
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Chicken of the Sea Solid White Tuna in Water
  • From: U.S. Dept. of Health & Human Services
• Tri-Union Seafoods Issues Precautionary, Voluntary Recall of Limited 12-Ounce Solid White Tuna in Water
  • From: U.S. Food & Drug Administration (FDA)
• The July 2010 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 30, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• FoodSafety.gov News & Events Update
  • From: U.S. Dept. of Health & Human Services
• Update of CVM's What's New - Storing, Handling and Using Animal Milk Replacer Products
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• NOAA, FDA, and Gulf Coast State Officials Affirm Commitment to Ensuring Safety of Gulf Coast Seafood
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Effexor Extended Release Capsules to Treat Major Depressive Disorder
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated MUMS Designation List and June 2010 Green Book Update
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• Update of CVM's What's New - Guidance for Industry and FDA: Advisory Levels for Deoxynivalenol (DON) in Grains and Grain By-Products used for Animal Feed
  • From: U.S. Food & Drug Administration (FDA)
• INZ Distributors Inc./Magic Power Coffee Inc. Conducts a Voluntary Nationwide Recall of Magic Power Coffee Dietary Supplement
  • From: U.S. Food & Drug Administration (FDA)
• Pure Base Distrbution Issues Allergy Alert on Undeclared Milk and Wheat in "Pure Base Garlic Spread - Concentrate" and "Pure Base Garlic Spread - Ready to Spread"
  • From: U.S. Food & Drug Administration (FDA)
• Kellogg Company Voluntarily Recalls Select Packages of Kellogg's® Corn Pops®, Kellogg's® Honey Smacks®, Kellogg's® Froot Loops® and Kellogg's® Apple Jacks®
  • From: U.S. Food & Drug Administration (FDA)
• P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Rapid Test for Antibodies to Hepatitis C Virus
  • From: U.S. Food & Drug Administration (FDA)
• Lancaster Foods, LLC Voluntarily Recalls Fresh Spinach with Best Enjoyed By Dates of June 19 to June 27, 2010 Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Anesthesiologist Sentenced on Health Care Fraud Charge
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Rapid blood test for antibodies to the hepatitis C virus (HCV) approved
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals
  • From: U.S. Food & Drug Administration (FDA)
• Two Recalls: Some Kellogg's Cereals and BBQ Chicken Pizza
  • From: U.S. Dept. of Health & Human Services
• H1N1 Influenza Public Health Emergency Determination to Expire on June 23
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• Office of Women's Health eUpdate
  • From: U.S. Food & Drug Administration (FDA)
• Two Recalls: Beef Products and Fresh Spinach
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
  • From: U.S. Food & Drug Administration (FDA)
• Advance Notice for Termination of the Emergency Use Authorization (EUA) of Medical Products and Devices
  • From: U.S. Dept. of Health & Human Services
• New CDC Test to Detect Human Infections with the 2009 H1N1 Influenza Virus Authorized for Use by FDA
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• Enforcement Report for June 23, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Upcoming Webinar June 29th at 11:00 am ET: FDA Center for Tobacco Products Inaugural Year and Looking Forward
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Extends Comment Period on the Advanced Notice of Proposed Rulemaking for the Veterinary Feed Directive Regulation
  • From: U.S. Food & Drug Administration (FDA)
• Three New Recalls: Ground Beef and Pet Vitamins
  • From: U.S. Dept. of Health & Human Services
• Update of CVM's What's New - United Pet Group Voluntarily Recalls Pro-Pet Adult Daily Vitamin Supplement for Dogs Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• United Pet Group Voluntarily Recalls Pro-Pet Adult Daily Vitamin Supplement for Dogs Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers to Avoid Magic Power Coffee
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• FDA Warns About Fraudulent Tamiflu
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• FDA to Hold Daylong Meeting on Medical Device Innovation
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Pfizer Voluntarily Withdraws Cancer Treatment Mylotarg from U.S. Market
  • From: U.S. Food & Drug Administration (FDA)
• Mylotarg (gemtuzumab ozogamicin): Market Withdrawal-Drug failed to demonstrate clinical benefit to patients enrolled in trials
  • From: FDA MedWatch
• RECALL: "Meat Without Feet" Lobster Claw & Knuckle Meat
  • From: U.S. Dept. of Health & Human Services
• FDA Marks First Anniversary of Tobacco Control Act
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Fourth Generation HIV Diagnostic Test Approved, permitting earlier detection of infection
  • From: U.S. Food & Drug Administration (FDA)
• Portland Shellfish Company Expands Recall to Include Meat Without Feet Label, Lobster Claw and Knuckle Meat, because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Diagnostic Assay to detect both HIV Antigen and Antibodies
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food Due to a Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magic Power Coffee: Undeclared Drug Ingredient - drug ingredient hydroxythiohomosildenafil may interact with prescription nitrates, and cause dangerously low blood pressure
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• PET FOOD RECALL: Natural Balance Sweet Potato & Chicken Dry Dog Food
  • From: U.S. Dept. of Health & Human Services
• Rich Products Corporation announces nationwide voluntary recall of Allen Bavarian Crème Filling due to undeclared allergens in product
  • From: U.S. Food & Drug Administration (FDA)
• Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food Due to a Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers to Avoid Magic Power Coffee
  • From: U.S. Food & Drug Administration (FDA)
• WHO Updates International H1N1 Flu Situation
  • From: U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• Update of CVM's What's New - Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Marie Callender's Cheesy Chicken & Rice, Possible Salmonella
  • From: U.S. Dept. of Health & Human Services
• Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products
  • From: U.S. Food & Drug Administration (FDA)
• FDA Fines American Red Cross $16 Million for Prior Failures to Meet Blood Safety Laws
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Treatment for Advanced Prostate Cancer
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Indication for Tasigna
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns About Fraudulent Tamiflu
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Three Varieties of Spaghettios With Meatballs
  • From: U.S. Dept. of Health & Human Services
• Tamiflu: Counterfeit Product Sold on Internet - contains undeclared cloxacillin; risk for those allergic to penicillins
  • From: FDA MedWatch
• Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count
  • From: U.S. Food & Drug Administration (FDA)
• Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 16, 2010
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• NIH-Funded Scientists Find 2009 H1N1 Pandemic Influenza Vaccine Protects Mice from 1918 Influenza Virus
  • From: U.S. Dept. of Health & Human Services
• FDA to Host Public Meeting on Oversight of Laboratory-Developed Tests
  • From: U.S. Food & Drug Administration (FDA)
• Strengthening the Health Care Workforce Through the Affordable Care Act
  • From: U.S. Dept. of Health & Human Services
• FDA to Communicate Safety Monitoring Activities to Consumers and Health Care Professionals
  • From: U.S. Food & Drug Administration (FDA)
• May 2010 Drug Safety Labeling Changes: 23 Medical Product Labels with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• FDA Cautions on Accurate Vitamin D Supplementation for Infants
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vitamin D Supplement Products: Medication Use Error - Some liquid Vitamin D supplements sold with droppers that could allow harmful amounts of Vitamin D to be dispensed
  • From: FDA MedWatch
• Portland Shellfish Company Recalls Cooked, Frozen Claw Island Brand, Craig's All Natural Brand And Inland Ocean Brand Lobster Claw And Knuckle Meat Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• FoodSafety.gov News & Events Update
  • From: U.S. Dept. of Health & Human Services
• Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes
  • From: U.S. Food & Drug Administration (FDA)
• NOAA, FDA Continue Ramping Up Efforts to Ensure Safety of Gulf of Mexico Seafood
  • From: U.S. Food & Drug Administration (FDA)
• Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen
  • From: U.S. Dept. of Health & Human Services
• Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk
  • From: U.S. Dept. of Health & Human Services
• Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The Melamine Story
  • From: U.S. Food & Drug Administration (FDA)
• Former Colorado Springs Pharmacist Sentenced for Importation and Distribution of Chinese-Made Human Growth Hormones and Conspiracy to Distribute Anabolic Steroids
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Benicar (olmesartan) Ongoing Safety Review - FDA evaluating data in which type 2 diabetes patients taking Benicar had a higher rate of death from cardiovascular cause compared to placebo. FDA has not concluded that Benicar increases the risk of death.
  • From: FDA MedWatch
• Domega NY International Co., LTD Issues Allergy Alert on Undeclared Egg in Fuma Custard Pie
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Seizes More Than $32,000 Worth of Bulk Honey from Philadelphia Distribution Center
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Brand Liposyn and Propofol: Recall - Injectable products may contain particulate matter.
  • From: FDA MedWatch
• FDA Advisory Panel to Review Dental Amalgam
  • From: U.S. Food & Drug Administration (FDA)
• How do I report a complaint about restaurant food?
  • From: U.S. Food & Drug Administration (FDA)
• How do I report a complaint about food bought in a supermarket?
  • From: U.S. Food & Drug Administration (FDA)
• How is the term "organic" regulated?
  • From: U.S. Food & Drug Administration (FDA)
• Does FDA have a definition for the term "organic" on food labels?
  • From: U.S. Food & Drug Administration (FDA)
• What is the meaning of 'natural' on the label of food?
  • From: U.S. Food & Drug Administration (FDA)
• If a food is labeled "organic" according to the USDA, is it still subject to the laws and regulations enforced by FDA?
  • From: U.S. Food & Drug Administration (FDA)
• Is Stevia an 'FDA approved' sweetener?
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - AHI Webinar - "Question-Based Review - Part II: Drug Product"
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1)
  • From: U.S. Food & Drug Administration (FDA)
• P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1)
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 9, 2010
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Defibtech DBP-2800 Battery Packs used in Lifeline AED and ReviveR AED: Recall
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
  • From: U.S. Food & Drug Administration (FDA)
• West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED^®and ReviveR AED^TM
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New article for veterinarians on Preventing Medication Errors in Animals
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - June 2010 FDA Patient Safety News now available
  • From: FDA MedWatch
• Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico
  • From: U.S. Dept. of Health & Human Services
• Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico
  • From: U.S. Food & Drug Administration (FDA)
• FDA Takes Action Against California Soy-Product Manufacturer Lifesoy
  • From: U.S. Food & Drug Administration (FDA)
• How did the Federal Food, Drug, and Cosmetic Act come about?
  • From: U.S. Food & Drug Administration (FDA)
• When and why was FDA formed?
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• The June 2010 FDA Patient Safety News is now available...
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GammaGard Liquid, Immune Globulin Intravenous (Human): Market withdrawal due to reports of allergic reactions
  • From: FDA MedWatch
• WHO Director-General Statement on Continuation of Pandemic Disease
  • From: U.S. Dept. of Health & Human Services
• Enforcement Report for June 2, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 2, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Minor Use Minor Species Drug Designation List Update
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Start of Generally Recognized as Safe (GRAS) Notification Pilot Program for Ingredients in Animal Food
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - May 2010 Green Book Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Basics Videos: Tim Coté on Orphan Drugs
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Preliminary Results: Surveillance for Guillain-Barre Syndrome After Receipt of Influenza A (H1N1) 2009 Monovalent Vaccine --- United States, 2009--2010
  • From: U.S. Dept. of Health & Human Services
• Kent Nutrition Group, Inc. Undertakes Limited Recall of Kent Feeds 20 Lamb DQ45 Medicated
  • From: U.S. Food & Drug Administration (FDA)
• Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Aquaculture and Aquaculture Drugs Basics article
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Injectable Osteoporosis Treatment for Postmenopausal Women
  • From: U.S. Food & Drug Administration (FDA)
• The June 2010 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks
  • From: U.S. Dept. of Health & Human Services
• HIV/AIDS Update - Selzentry (maraviroc) 150 mg and 300 mg tablets, labeling changes for patients with renal impairment
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 26, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks
  • From: U.S. Food & Drug Administration (FDA)
• Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children's Products
  • From: U.S. Food & Drug Administration (FDA)
• PediaCare Children's Products [Blacksmith Brand]: Recall of four products - The four products were manufactured at a plant cited by FDA for deficiencies in Good Manufacturing Practices
  • From: FDA MedWatch
• Intravenous Medications Manufactured by Claris-Metronidazole, Ciprofloxacin and Ondansetron:Recall due to contamination of products
  • From: FDA MedWatch
• Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn[TM] and Propofol That May Contain Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• Fraud Prevention & The Affordable Care Act
  • From: U.S. Dept. of Health & Human Services
• Wally's Nut House, LLC Issues Allergy Alert on Undeclared Milk, Soy, and Wheat
  • From: U.S. Dept. of Health & Human Services
• organicgirl Produce Announces Limited Precautionary Recall of 10 oz organicgirl Baby Spinach with Use-by Date of May 22 Due to Possible Health Concern
  • From: U.S. Dept. of Health & Human Services
• Wally's Nut House, LLC ISSUES ALLERGY ALERT ON UNDECLARED MILK, SOY, AND WHEAT IN THE FOLLOWING PRODUCTS: "Tailgate Crunch Mix, Sweet Cajun Heat Mix, Country Western Mix, Cranberry Raisin Mix, Party Mix, Hot 'n Spicy Mix, and Louisiana Cajun Mix"
  • From: U.S. Food & Drug Administration (FDA)
• organicgirl Produce Announces Limited Precautionary Recall of 10 oz organicgirl Baby Spinach with Use-by Date of May 22 Due to Possible Health Concern
  • From: U.S. Food & Drug Administration (FDA)
• Herb And Honey Issues Alert On Undeclared Sulfites In "Dried Apricots"
  • From: U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update
  • From: U.S. Dept. of Health & Human Services
• Herb And Honey Issues Alert On Undeclared Sulfites In "Dried Apricots"
  • From: U.S. Food & Drug Administration (FDA)
• So Shing Hing (USA) Trading Co Ltd Issues an Alert on Undeclared Sulfites in Dried Melon
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Rare Cases of Liver Injury Reported with Use of Xenical, Alli
  • From: U.S. Food & Drug Administration (FDA)
• FDA Announces Collaboration with Drugs.com
  • From: U.S. Food & Drug Administration (FDA)
• So Shing Hing (USA) Trading Co Ltd Issues an Alert on Undeclared Sulfites in Dried Melon
  • From: U.S. Dept. of Health & Human Services
• Hylenex recombinant (hyaluronidase human injection): Recall - Voluntary recall of all manufactured lots has been initiated as a precautionary measure due to instances of particulate matter observed in a limited number of vials during routine stability testing.
  • From: FDA MedWatch
• FDA MedWatch - Orlistat (marketed as Alli and Xenical): Labeling Change
  • From: FDA MedWatch
• Update of CVM's What's New - 2011: World Veterinary Year
  • From: U.S. Food & Drug Administration (FDA)
• HealthReform.gov Blog Update
  • From: U.S. Dept. of Health & Human Services
• FDA: Possible Fracture Risk with High Dose, Long-term Use of Proton Pump Inhibitors
  • From: U.S. Food & Drug Administration (FDA)
• Western District of Wisconsin Announces Consent Decree Between Beehive Botanicals and the United States
  • From: U.S. Food & Drug Administration (FDA)
• FoodSafety.gov News & Events Update
  • From: U.S. Dept. of Health & Human Services
• FDA MedWatch - Proton Pump Inhibitors (PPI): Class Labeling Change
  • From: FDA MedWatch
• FDA Approves New Treatment for Late-Onset Pompe Disease
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ultram (tramadol hydrochloride), Ultracet (tramadol hydrochloride/acetaminophen): Label Change
  • From: FDA MedWatch
• Fresh Express Recalls Romaine-based Salads with Use-by Dates of May 13-16th Due to Possible Health Risk
  • From: U.S. Dept. of Health & Human Services
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Medicare & the Affordable Care Act
  • From: U.S. Dept. of Health & Human Services
• Fresh Express Recalls Romaine-based Salads with Use-by Dates of May 13-16th Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FoodSafety.gov News & Events Update
  • From: U.S. Dept. of Health & Human Services
• Weekly FluView Map and Surveillance Report for the Week Ending May 15, 2010
  • From: U.S. Dept. of Health & Human Services
• FDA Clears First 2009 H1N1 Influenza Virus Test Previously Available Under Emergency Use Authorization
  • From: U.S. Dept. of Health & Human Services
• Update of CVM's What's New - FDA and NIH Launch Electronic Safety Reporting Portal
  • From: U.S. Food & Drug Administration (FDA)
• Genzyme Corp. Signs Consent Decree to Correct Violations at Allston, Mass., Manufacturing Plant and Give up $175 Million in Profits
  • From: U.S. Food & Drug Administration (FDA)
• FDA and NIH Launch Electronic Safety Reporting Portal
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces the Availability of Electronic Submissions for Animal Drug Adverse Events/New Guidance Available
  • From: U.S. Food & Drug Administration (FDA)
• Watch: FDA Basics Videos
  • From: U.S. Food & Drug Administration (FDA)
• How many people are employed by FDA and in what areas do they work?
  • From: U.S. Food & Drug Administration (FDA)
• Ortho-McNeil Pharmaceutical, LLC Pleads Guilty to Illegal Promotion of Topamax and is Sentenced to Criminal Fine of $6.14 Million
  • From: U.S. Food & Drug Administration (FDA)
• FDA Clears First 2009 H1N1 Influenza Virus Test Previously Approved for Emergency-Use Only
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA Basics Updates - Webinar on May 26 at 2:00pm ET
  • From: U.S. Food & Drug Administration (FDA)
• Caldwell Fresh Foods Recalls Alfalfa Sprouts Because of Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• Urgent Nationwide Alfalfa Sprout Recall
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Urgent Nationwide Alfalfa Sprout Recall
  • From: U.S. Dept. of Health & Human Services
• HIV/AIDS Update - June 10-11, 2010 Advisory Committee meeting re: policy on deferral of donors with high-risk exposure to HIV
  • From: U.S. Food & Drug Administration (FDA)
• CORRECTION: Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes"
  • From: U.S. Dept. of Health & Human Services
• Vanlaw Food Products, Inc. Announces Voluntary Recall of Valu Time Brand Ranch Dressing
  • From: U.S. Dept. of Health & Human Services
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes"
  • From: U.S. Dept. of Health & Human Services
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Egg in "Peanut Butter Spread"
  • From: U.S. Dept. of Health & Human Services
• Voluntary Recall of HYLENEX Initiated
  • From: U.S. Food & Drug Administration (FDA)
• How do I discard medicine that I no longer need, do I just throw it in the garbage?
  • From: U.S. Food & Drug Administration (FDA)
• What are unapproved drugs and why are they on the market?
  • From: U.S. Food & Drug Administration (FDA)
• Vanlaw Food Products, Inc. Announces Voluntary Recall of Valu Time Brand Ranch Dressing
  • From: U.S. Food & Drug Administration (FDA)
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes"
  • From: U.S. Food & Drug Administration (FDA)
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Egg in "Peanut Butter Spread"
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Launches Initiative to Reduce Infusion Pump Risks
  • From: U.S. Food & Drug Administration (FDA)
• FDA Launches Initiative to Reduce Infusion Pump Risks
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 21, 2010
  • From: U.S. Food & Drug Administration (FDA)
• LIFEPAK 15 Monitor/Defibrillator by Physio-Control Inc.-Class I Recall
  • From: FDA MedWatch
• CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Announces Draft Revised Guidance on Transparency and Advisory Committees
  • From: U.S. Food & Drug Administration (FDA)
• Propylthiouracil-Boxed Warning Added
  • From: FDA MedWatch
• Federal Prisoner Serving Time for Health Care Fraud Charged with Distributing Misbranded Drugs that were Labeled as "All Natural" Sexual Enhancement
  • From: U.S. Food & Drug Administration (FDA)
• Buckley Woman Sentenced to Jail Time, Home Detention for False Claim of Glass in Bottled Water
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - New Boxed Warning on severe liver injury with propylthiouracil
  • From: U.S. Food & Drug Administration (FDA)
• FDA Announces Draft Revised Guidance on Transparency and Advisory Committees
  • From: U.S. Food & Drug Administration (FDA)
• Generic Drug Roundup: April 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA Obtains Consent Decree to Stop Marketing of Unapproved Sterilization System
  • From: U.S. Food & Drug Administration (FDA)
• No Bones About It: Bones are Unsafe for Your Dog
  • From: U.S. Food & Drug Administration (FDA)
• FDA Statement on IOM Sodium Report
  • From: U.S. Food & Drug Administration (FDA)
• FDA to Address Challenges of Using Complex Medical Devices in the Home
  • From: U.S. Food & Drug Administration (FDA)
• Upcoming Webinar on Thursday, April 22--Safeguarding the U.S. Food Supply: Excellent Industry Compliance With the Bovine Spongiform Encephalopathy (BSE) Final Rule
  • From: U.S. Food & Drug Administration (FDA)
• Purina Mills Undertakes Limited Recall of Strategy® Horse Feed and Layena® Poultry Feed
  • From: U.S. Food & Drug Administration (FDA)
• FDA Seeks Injunction Against Florida Animal Drug Compounder
  • From: U.S. Food & Drug Administration (FDA)
• FDA Launches Medical Device and Radiation-Emitting Product Transparency Web site
  • From: U.S. Food & Drug Administration (FDA)
• ***CONSUMER ALERT*** Undeclared Sulfites in "Nut Tree Health Mix"
  • From: U.S. Food & Drug Administration (FDA)
• StarKist Co. Initiates Limited Regional Voluntary Recall of Two SeaSations® Products Due to Undeclared Allergen
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Guidance on New Safety Rules for Shell Eggs
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 14, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2010 Drug Safety Labeling Changes: 40 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• My-A & Co, Recalls Ground Black Pepper Double Golden Fish 3.5oz Jars Due to Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Atlas Operations, Inc. Announces Expansion of its Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update
  • From: U.S. Food & Drug Administration (FDA)
• Response Products Voluntarily Recalls Advanced Cetyl M Joint Action Formula for Dogs Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Asthma and COPD Inhalers That Contain Ozone-depleting CFCs to be Phased Out; Alternative Treatments Available
  • From: U.S. Food & Drug Administration (FDA)
• Seven Inhalers That Use CFCs Being Phased Out
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves Pancreatic Enzyme Product, Pancreaze
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Pancreatic Enzyme Product, Pancreaze
  • From: U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: March 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Holds Public Meeting on Prescription Drug User Fee Act
  • From: U.S. Food & Drug Administration (FDA)
• Consumer Alert Precautionary Recall issued for H-E-B French Onion Dip
  • From: U.S. Food & Drug Administration (FDA)
• FDA Holds Public Meeting on Prescription Drug User Fee Act
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meeting on the National Antimicrobial Resistance Monitoring System (NARMS)
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - April 2010 FDA Patient Safety News now available
  • From: FDA MedWatch
• Drug Information Update: FDA Provides Information to Consumers about the Ingredient Triclosan
  • From: U.S. Food & Drug Administration (FDA)
• Mccormick & Company Recalls Mccormick Fajitas Seasoning Mix Due To Unlabeled Wheat And Milk Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• FDA Provides Information to Consumers about Triclosan
  • From: U.S. Food & Drug Administration (FDA)
• Triclosan: What Consumers Should Know
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves First Generic Versions of Two Drugs for the Treatment of Hypertension
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Versions of Two Drugs for the Treatment of Hypertension
  • From: U.S. Food & Drug Administration (FDA)
• Camolyn eye drops, Fisiolin nasal drops: Voluntary recall :Lack of sterile product has the potential to cause infections
  • From: FDA MedWatch
• Stud Capsule For Men: Product adulterated with sildenafil which may interact with nitrates to lower blood pressure to dangerous levels
  • From: FDA MedWatch
• US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles.
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 7, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns About Lipodissolve Product Claims
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Issues Warning Letters for Drugs Promoted in Fat Elimination Procedure
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Warning Letters for Drugs Promoted in Fat Elimination Procedure
  • From: U.S. Food & Drug Administration (FDA)
• Medical Device Manufacturer Guidant Pleads Guilty for not Reporting Defibrillator Safety Problems to FDA
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: Follow up to the Public Health Alert about Changes to the Heparin Sodium USP Monograph
  • From: U.S. Food & Drug Administration (FDA)
• Kroger Recalls Two Seasonings Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Del Bueno Recalls Queso Fresco Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Del Bueno Amends Recall of Queso Fresco Cheese Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Kanec USA Inc., Issues a Voluntary Nationwide Recall of Stud Capsule For Men Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Frozen Whole Catch Yellow Fin Tuna Steaks Due to Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Formulation for OxyContin
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves New Formulation for OxyContin
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Biodegradable Sealant Patch for Cardiovascular Surgery
  • From: U.S. Food & Drug Administration (FDA)
• Federal Government Seizes Dozens of Misbranded Drug Products
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - March 2010 Update on Feed Enforcement Activities to Limit the Spread of BSE
  • From: U.S. Food & Drug Administration (FDA)
• Golden Pacific Foods, Inc. Issues Allergy Alert for Undeclared Milk and Soy in Marco Polo Brand Shrimp Snacks
  • From: U.S. Food & Drug Administration (FDA)
• NY Gourmet Salads Inc. Recalls Chick Pea Salad Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Consumer Representatives Needed for FDA Advisory Committees: Learn More at Public Meeting
  • From: U.S. Food & Drug Administration (FDA)
• Glutino Food Group Issues Allergy Alert on Undeclared Egg Product in Raisin Bread
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 31, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Zatarain's Recalls Original Dirty Rice Mix Package Due to Unlabeled Wheat and Barley Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• Watkins Incorporated Recalls Crab Snack & Dip Seasoning Because of Possible Health Risk from Ingredient Supplied by Kerry Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• Federal Government Seeks Permanent Injunction Against Texas Egg Roll Manufacturer
  • From: U.S. Food & Drug Administration (FDA)
• FDA Requires Device Manufacturers to Include Information on Pediatric Populations
  • From: U.S. Food & Drug Administration (FDA)
• Stalevo (entacapone/carbidopa/levodopa): Ongoing Safety Review
  • From: FDA MedWatch
• Drug Information Update - Ongoing Safety Review of Stalevo (entacapone/carbidopa/levodopa) and possible development of Prostate Cancer
  • From: U.S. Food & Drug Administration (FDA)
• Binell Bros. Cutlery Voluntarily Recalls Black Pepper
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Asclera to Treat Small Varicose Veins
  • From: U.S. Food & Drug Administration (FDA)
• MasXtreme Capsules (Natural Wellness) - product contains undeclared drug ingredient
  • From: FDA MedWatch
• FDA Approves Asclera to Treat Small Varicose Veins
  • From: U.S. Food & Drug Administration (FDA)
• Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed As a Dietary Supplement
  • From: U.S. Food & Drug Administration (FDA)
• Modern Products recalls Seasonings due to possible health risk
  • From: U.S. Food & Drug Administration (FDA)
• Perfect Candy & Packaging Co. Announces a Voluntary Nationwide Recall of Whole Black Pepper in H.D.W. FOODS Labeled Bags
  • From: U.S. Food & Drug Administration (FDA)
• Medications for Your Pet: 10 Questions to Ask Your Vet
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Solicits Comments Related to Veterinary Feed Directive (VFD) Drugs
  • From: U.S. Food & Drug Administration (FDA)
• Public Health Agencies Collaborate to Prevent Further Illnesses from Norovirus Outbreak Associated with Oysters Recently Harvested from Area Near Port Sulphur, La.
  • From: U.S. Food & Drug Administration (FDA)
• Two Arrested for Illegally Trafficking Counterfeit Weight Loss Medication
  • From: U.S. Food & Drug Administration (FDA)
• Public Health Agencies Warn of Outbreaks Related to Drinking Raw Milk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Takes Action Against New York Dairy Farmer
  • From: U.S. Food & Drug Administration (FDA)
• Obstetrics Manager Convicted of Tampering with Patient's Narcotics Medicines at White Salmon Hospital
  • From: U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Voluntary Nationwide Recall of Chilli Man Seasoning Mix due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Amended Voluntary Nationwide Recall of several additional products that contain pepper due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves New Use of Xifaxan for Patients with Liver Disease
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Use of Xifaxan for Patients with Liver Disease
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 24, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Blue Line Foodservice Distribution voluntarily recalls "Spice Paks"
  • From: U.S. Food & Drug Administration (FDA)
• Walong Marketing, Inc. Expands Nationwide Voluntary Recall Flying Horse Sesame Chewy Candy Due to Undeclared Peanuts
  • From: U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Amended Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• McCain Foods USA Announces Voluntary Recall of Frozen Potato Product Containing Black Pepper That May Pose Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Rotarix Vaccine: Recommendation to suspend use-Precaution while FDA learns more about the situation. No known safety risk at this time
  • From: FDA MedWatch
• U.S. Attorney News Release: Three Indicted for Diversion of Prescription Drugs
  • From: U.S. Food & Drug Administration (FDA)
• Components of Extraneous Virus Detected in Rotarix Vaccine; No Known Safety Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Drug Info: Drug Safety Podcasts for Healthcare Professionals
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Springfield (Missouri) Business Owner Pleads Guilty to $17 Million Fraud Scheme
  • From: U.S. Food & Drug Administration (FDA)
• John B. Sanfilippo & Son, Inc. Voluntarily Recalls Snack Mix and Cashew Products Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Upcoming Webinar on FDA's Inspection Process
  • From: U.S. Food & Drug Administration (FDA)
• Boston Scientific Implantable Cardioverter Defibrillators:Recall-Practitioners should not use devices unless, until FDA reviews, approves changes made by the manufacturer
  • From: FDA MedWatch
• Zocor (simvastatin): increased risk of muscle injury with high doses-risk also increased when drug, especially at higher doses, is used with certain drugs
  • From: FDA MedWatch
• Kroger Amends Code Date on Recalled Seasoning Blend Garlic Powder
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Warns about Increased Risk of Muscle Injury with Zocor
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns about Increased Risk of Muscle Injury with Zocor
  • From: U.S. Food & Drug Administration (FDA)
• Becton, Dickinson (BD) Q-Syte Luer Access Split Septum Device: Class I Recall-Defective devices may result in air bubbles leaking into the infusion system and into the patient's bloodstream
  • From: FDA MedWatch
• Drug Information Update- FDA Approves Carbaglu Tablets to Treat Condition That Causes Elevated Ammonia Levels.
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Drug to Treat Condition That Causes Elevated Ammonia Levels
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Final Rule Restricting Access and Marketing of Cigarettes and Smokeless Tobacco Products to Youth
  • From: U.S. Food & Drug Administration (FDA)
• Cleviprex (clevidipine butyrate): Recall of 12/2009 expanded to additional lots; Presence of particulate matter could reduce blood flow...
  • From: FDA MedWatch
• Enforcement Report for March 17, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 17, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Barcel Announces Voluntary Recall
  • From: U.S. Food & Drug Administration (FDA)
• Produce Valley, Inc. Initiates Voluntary Recall Due to Possible Health Risk Associated with Recalled Hydrolyzed Vegetable Protein (HVP) by Basic Food Flavors, Inc.
  • From: U.S. Food & Drug Administration (FDA)
• Statement for National Poison Prevention Week
  • From: U.S. Food & Drug Administration (FDA)
• Spice Barn, Inc. Voluntarily Recalls Two Lots of Black Pepper
  • From: U.S. Food & Drug Administration (FDA)
• The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Gyrus ACMI Micron Bobbin Vent Tube T: Class I Recall-Device implanted for ventilation or drainage of the middle ear - shipped without being sterilized
  • From: FDA MedWatch
• FDA Approves First Totally Implanted Hearing System
  • From: U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: February 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA Seeks Permanent Injunction Against Louisiana Sprout Grower
  • From: U.S. Food & Drug Administration (FDA)
• FDA March 17 Update on the Investigation into the Salmonella Montevideo Outbreak
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets
  • From: U.S. Food & Drug Administration (FDA)
• FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets
  • From: U.S. Food & Drug Administration (FDA)
• GFN Foods, LLC Voluntarily Recalls Gluten-Free Naturals Pancake Mix, Gluten-Free Naturals Light & Moist Yellow Cake Mix and Gluten-Free Naturals Cookie Blend Flour
  • From: U.S. Food & Drug Administration (FDA)
• Emmi - Roth Käse USA Announces Recall of Spreadables brand Crab Creole and Shrimp Scampi Cheese Spreads
  • From: U.S. Food & Drug Administration (FDA)
• Teleflex Arrow IV Tubing Sets, Accessories, and Embolectomy Catheters: Recall
  • From: FDA MedWatch
• Start at the Store: Prevent Foodborne Illness (video)
  • From: U.S. Food & Drug Administration (FDA)
• Tastefully Simple Issues Voluntary Recall for Toasted Garlic & Parmesan Cheese Ball Mix
  • From: U.S. Food & Drug Administration (FDA)
• Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters
  • From: U.S. Food & Drug Administration (FDA)
• Julia's Spices Inc Recalls Hulled Sesame Seeds Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Spice Industrial Inc. Recalls Lian How White Sesame Seeds Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: Statement to Healthcare Professionals on the ACCORD Lipid Trial
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 10, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Plavix (clopidogrel): Boxed warning added regarding reduced effectiveness of Plavix in poor metabolizers
  • From: FDA MedWatch
• Counterfeit Polypropylene Surgical Mesh: Counterfeit flat sheets of product are being marketed US, labeled with Bard/Davol brand name
  • From: FDA MedWatch
• FDA Announces New Boxed Warning on Plavix
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Reduced effectiveness of Plavix (clopidogrel) in patients who are poor metabolizers of the drug
  • From: U.S. Food & Drug Administration (FDA)
• FDA Task Force Seeks Public Comments on Increasing Transparency with Regulated Industry
  • From: U.S. Food & Drug Administration (FDA)
• Austinuts Of Dallas, Inc. Announces Voluntary Recall of Honey Mustard Pretzels
  • From: U.S. Food & Drug Administration (FDA)
• McCormick Recall Due to Possible Health Risk from HVP Ingredient Expands to Include Additional "Best By" Dates
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Warning on Counterfeit Surgical Mesh
  • From: U.S. Food & Drug Administration (FDA)
• Abiomed AB5000 Circulatory Support System: Class I Recall-Device computer may shut down without an alarm, which can lead to serious injuries or death
  • From: FDA MedWatch
• Baylis Medical Torflex Transseptal Guiding Sheath: Class I Recall- tip may break off, separate during procedures, could lead to permanent injury and/or death
  • From: FDA MedWatch
• Oral Bisphosphonates:Ongoing Safety Review of Atypical Subtrochanteric Femur Fractures-have not shown clear connection between bisphosphonates, risk of fracture
  • From: FDA MedWatch
• Beckman Coulter UniCel DxC Synchron Clinical System - Ion Selective Electrode Flow Cell: Class I Recall-Incorrect sodium results due to build-up of protein, bacteria, in the flow cell
  • From: FDA MedWatch
• FDA March 11 Update on the Investigation into the Salmonella Montevideo Outbreak
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2010 Drug Safety Labeling Changes: 24 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• Orval Kent Food Company, Inc. Voluntarily Recalls Culinary Circle Dips Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Black Pepper
  • From: U.S. Food & Drug Administration (FDA)
• Olde Westport Spice Announces a Voluntary Recall of Garden Harvest Special Blend Seasoning
  • From: U.S. Food & Drug Administration (FDA)
• Mrs. Gerry's Kitchen Press Release
  • From: U.S. Food & Drug Administration (FDA)
• Quaker Snack Mix Baked Cheddar Voluntarily Recalled Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Mrs. Gerry's Kitchen Press Release.
  • From: U.S. Food & Drug Administration (FDA)
• Kroger Recalls Two Onion Soup & Dip Mixes Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Ventura Foods, LLC Voluntarily Recalls Seven Varieties of Its Dean's® Dip Products As A Precautionary Measure
  • From: U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Four Seasoning Mixes
  • From: U.S. Food & Drug Administration (FDA)
• P&G Joins Industry Ingredient Recall by Voluntarily Recalling Two Flavors of Pringles® in the United States in Response to FDA Industry Guidance
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Ongoing safety review of oral bisphosphonates and atypical subtrochanteric femur fractures
  • From: U.S. Food & Drug Administration (FDA)
• WinRho SDF (Rho(D) Immune Globulin Intravenous (Human): Risk of intravascular hemolysis in patients treated for immune thrombocytopenic purpura
  • From: FDA MedWatch
• Nutritional Resources Announces a Nationwide Voluntary Recall of Healthwise Cream of Mushroom Soup Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• GNS Foods Voluntarily Recalls Snack Mixes Containing Honey Mustard/Onion Pretzels from National Pretzel Co. associated with Hydrolyzed Vegetable Protein (HVP) recalled by Basic Food Flavors, Inc. because of the potential Salmonella contamination.
  • From: U.S. Food & Drug Administration (FDA)
• Herr Foods Inc. Recalls 'Herr's Cracked Pepper and Sea Salt Flavored' Kettle Style Potato Chips Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Black Pepper and Products made with Black Pepper
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Botox to Treat Spasticity in Flexor Muscles of the Elbow, Wrist and Fingers
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Botox to Treat Spasticity in Flexor Muscles of the Elbow, Wrist and Fingers
  • From: U.S. Food & Drug Administration (FDA)
• Nature's Variety Expands Nationwide Voluntary Recall to Include All Raw Frozen Chicken Diets with Any "Best If Used By" Date On or Before 2/5/11
  • From: U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Recalls Old Apple Tree Tomme Cheese Due to Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• National Pretzel Co. Annouces Precautionary Recall of Honey Mustard Onion Seasoned Pretzels Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Ed Roller, Inc. Announces Voluntary Recall of Wegmans 9 oz. Food You Feel Good About® Medium Seafood Sauce Due to Undeclared Ingredients on Label
  • From: U.S. Food & Drug Administration (FDA)
• Fresh Food Concepts Announces a Voluntary Recall of Spinach Dips Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• McCormick & Company Initiates Recall Due to Possible Health Risk from HVP Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• Creative Contract Packaging Corporation Recalls HERB-OX® Bouillon Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Mincing Overseas Spice Company Voluntarily Recalls Two Lots of Black Pepper
  • From: U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - March 5, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Concord Foods Recalls Concord Foods Seasonings Mixes because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Thomas Medical Products, Inc., Transseptal Sheath Introducer Kits: Class I Recall
  • From: FDA MedWatch
• Recall of Hydrolyzed Vegetable Protein
  • From: U.S. Food & Drug Administration (FDA)
• FDA Investigation Reveals Salmonella Tennessee at Plant that Makes Flavor Enhancers for Food Processors and Other Distributors
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Name Change for Heartburn Drug Kapidex
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Name Change for Heartburn Drug Kapidex
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2010 FDA Patient Safety News now available
  • From: FDA MedWatch
• Baxter HomeChoice and HomeChoice PRO Automated Peritoneal Dialysis Systems: Class I Recall. Reports of serious injuries associated with increased Intraperitoneal Volume
  • From: FDA MedWatch
• Reser's Fine Foods Inc Press Release
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Warns Consumers in Puerto Rico of Harmful Bacteria in Hand Sanitizers
  • From: U.S. Food & Drug Administration (FDA)
• Earth Island Announces Voluntary Recall On Select Follow Your Heart Products That Contain Natural Flavor Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Homemade Gourmet Voluntarily Recalls "Tortilla Soup Mix" Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers in Puerto Rico of Harmful Bacteria in Hand Sanitizers
  • From: U.S. Food & Drug Administration (FDA)
• FDA, FSIS, CDC Collaborate on Methods to Measure Success of Food Safety Programs
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 3, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA Calls on Food Companies to Correct Labeling Violations; FDA Commissioner Issues an Open Letter to the Industry
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 24, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves First Generic Tamsulosin to Treat Enlarged Prostate Gland
  • From: U.S. Food & Drug Administration (FDA)
• Castella Imports, Inc. Conducts Nationwide Recall of Castella Chicken Soup Base Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Survey Finds More Americans Read Information on Food Labels
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Tamsulosin to Treat Enlarged Prostate Gland
  • From: U.S. Food & Drug Administration (FDA)
• Survey Shows Gains in Food-Label Use, Health/Diet Awareness
  • From: U.S. Food & Drug Administration (FDA)
• T. Marzetti Company Announces a Voluntary Recall of Dips Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Boca Raton Man Sentenced for Nutritional Supplement Scam
  • From: U.S. Food & Drug Administration (FDA)
• Heartland Foods, Inc. voluntarily recalls Coarse Ground Black Pepper because of possible Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• FDA Announces Meeting Information and Voting Membership of the Tobacco Products Scientific Advisory Committee
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Therapy to Treat Gaucher Disease
  • From: U.S. Food & Drug Administration (FDA)
• American Pecan Co. Recalls Pecans Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Johnny's Fine Foods Recalls Johnny's French Dip Powdered Au Jus Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• International Collaboration: FDA and European Medicines Agency Agree to Accept a Single Orphan Drug Designation Annual Report
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Therapy to Treat Gaucher Disease
  • From: U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 26, 2010
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Medical Device Manufacturer Guidant Charged in Failure to Report Defibrillator Safety
  • From: U.S. Food & Drug Administration (FDA)
• OneTouch SureStep Test Strips: Recall-Test strips may provide falsely low results when glucose level is over 400 mg/dL
  • From: FDA MedWatch
• StatSpin Express 4 Centrifuges: Recall- Rotor may break, eject pieces of the rotor, may cause serious physical injury, expose to blood-borne infectious micro-organisms
  • From: FDA MedWatch
• Thumb Oilseed Recalls Soy Grits and Flour Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• LifeScan Recalls Specific Lots of Consumer and Professional OneTouch® SureStep® Test Strips Due To Inaccurate
  • From: U.S. Food & Drug Administration (FDA)
• Wholesome Spice Recalls 25 Lb. Boxes Of Crushed Red Pepper Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Trader Joe's Company Voluntarily Recalls Chocolate Chip Chewy Coated Granola Bars
  • From: U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 25, 2010
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Medical Technician Sentenced to 30 Years
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 24, 20104
  • From: U.S. Food & Drug Administration (FDA)
• Maryland Veal Calf Dealer Agrees to Close in Response to FDA-Initiated Action
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Pneumococcal Disease Vaccine with Broader Protection
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: Mifeprex Questions and Answers
  • From: U.S. Food & Drug Administration (FDA)
• NIH and FDA Announce Collaborative Initiative to Fast-track Innovations to the Public
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Woman pleads guilty to poisoning salsa at Lenexa restaurant
  • From: U.S. Food & Drug Administration (FDA)
• Reporting Problems to FDA (video)
  • From: U.S. Food & Drug Administration (FDA)
• Invirase (saquinavir): Ongoing safety review of clinical trial data-Possible association with abnormal heart rhythms when used in combination with Norvir (ritonavir)
  • From: FDA MedWatch
• FDA Announces Possible Safety Concern for HIV Drug Combination
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Ongoing safety review of Invirase (saquinavir) and possible association with abnormal heart rhythms
  • From: U.S. Food & Drug Administration (FDA)
• Safety Review of Avandia (Rosiglitazone)
  • From: U.S. Food & Drug Administration (FDA)
• Avandia (rosiglitazone): FDA reviewing a large, long-term clinical study on possible risks for cardiovascular outcomes with use of rosiglitazone
  • From: FDA MedWatch
• Drug Information Update: Ongoing review of Avandia (rosiglitazone) and cardiovascular safety
  • From: U.S. Food & Drug Administration (FDA)
• Lovin Oven LLC Voluntarily Recalls Certain Health Valley® Organic Peanut Crunch, Dutch Apple and Wildberry Chewy Granola Bars
  • From: U.S. Food & Drug Administration (FDA)
• Fresh & Easy Neighborhood Market Voluntarily Recalls Fresh & Easy Chewy Chocolate Chip Granola Bars Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Lovin Oven LLC Voluntarily Recalls Certain Health Valley® Organic Peanut Crunch, Dutch Apple and Wildberry Chewy Granola Bars
  • From: U.S. Food & Drug Administration (FDA)
• Queseria Bendita Recalls Queso Fresco, Panela, and Requeson Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Regulatory Science Update: FDA and International Serious Adverse Events Consortium Complete Third Data Release
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Miami Prescription Drug Diverter Sentenced To 70 Months In Prison
  • From: U.S. Food & Drug Administration (FDA)
• Ear Candles: Risk of Serious Injuries-Consumers warned not to use ear candles because they can cause burns, perforation, blockage
  • From: FDA MedWatch
• Upcoming Webinar to Inform Public About Access to Investigational Drugs
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2010 Drug Safety Labeling Changes: 36 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• Drug Information Update- February 28, 2010 Deadline to Submit Comments on "Promotion of FDA-Regulated Medical Products Using the Internet and Social Media Tools"
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: SK Foods former owner charged with RICO violations
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Rituxan to Treat Chronic Lymphocytic Leukemia
  • From: U.S. Food & Drug Administration (FDA)
• FDA Cancer Drug Approval Rate Highlighted in JNCI
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Rituxan to Treat Chronic Lymphocytic Leukemia
  • From: U.S. Food & Drug Administration (FDA)
• USDA and FDA Coordinating Efforts to Ensure Safety of Produce
  • From: U.S. Food & Drug Administration (FDA)
• Long-Acting Beta-Agonists (LABAs): New Safe Use Requirements-FDA requires risk management plan and class-labeling changes for all LABAs
  • From: FDA MedWatch
• Don't Get Burned: Stay Away From Ear Candles
  • From: U.S. Food & Drug Administration (FDA)
• FDA Urges Safe Use of Certain Inhaled Asthma Medicines
  • From: U.S. Food & Drug Administration (FDA)
• Exjade (deferasirox): Boxed Warning - Changes to Prescribing Information re: risk of renal impairment/failure, hepatic impairment/failure or gastrointestinal hemorrhage
  • From: FDA MedWatch
• FDA Announces New Safety Controls for Long-Acting Beta Agonists, Medications Used to Treat Asthma
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - New safety requirements for long-acting inhaled asthma medications called Long-Acting Beta-Agonists (LABAs)
  • From: U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Expands Recall Of Various Cheeses Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns about Serious Side Effects from Maalox Product Mix-Ups
  • From: U.S. Food & Drug Administration (FDA)
• Maalox Total Relief: Medication Use Errors- Consumers with history of GI ulcers or bleeding disorder should not use product because it contains substance related to aspirin
  • From: FDA MedWatch
• Avoid Maalox Mix-Ups
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Drug Safety Communication: Product Confusion with Maalox Total Relief and Maalox Liquid Products
  • From: U.S. Food & Drug Administration (FDA)
• Walong Marketing, Inc. Issues Nationwide Voluntary Recall of Flying Horse Black and White Sesame Chewy Candy Due to Undeclared Peanuts
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 17, 2010
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces Animal Health Twitter Account
  • From: U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak
  • From: U.S. Food & Drug Administration (FDA)
• Erythropoiesis-Stimulating Agents (ESAs): Requirement that only hospitals and healthcare professionals who have enrolled, completed training in risk mgmt program will prescribe, dispense ESAs to patients with cancer
  • From: FDA MedWatch
• FDA Announces New Safety Plan for Agents Used to Treat Chemotherapy-Related Anemia
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Drug Safety Communication: Erythropoiesis-Stimulating Agents (ESAs): Procrit, Epogen and Aranesp
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Company pleads guilty to felony misbranding of a drug
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Subject sentenced to 51 months for sale of unapproved medical devices
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Business Owner Pleads Guilty to Fraudulently Marketing Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Nature's Variety Issues Nationwide Voluntary Recall On Raw Frozen Chicken Diets With A "Best If Used By" Date Of 11/10/10
  • From: U.S. Food & Drug Administration (FDA)
• Trader Joe's Company Voluntarily Recalls Chocolate Chip Chewy Coated Granola Bars
  • From: U.S. Food & Drug Administration (FDA)
• Stop & Shop Removes from Sale 24oz. Party Platter Cookies, Products Recalled Due to an Undeclared Allergen
  • From: U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Recalls Red Darla Cheese Due to Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• There will be no Enforcement Report for February 10, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Giant Food Recalls 24 oz. Party Platter Cookies
  • From: U.S. Food & Drug Administration (FDA)
• Cardiac Science Automated External Defibrillators (Powerheart, Cardiovive, CardioLife models): Recall- Device may not be able to deliver therapy during a cardiac resuscitation attempt
  • From: FDA MedWatch
• BD Q-Syte Luer Access Devices: Recall-Device may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death
  • From: FDA MedWatch
• Acacia, Inc. Announces Worldwide Voluntary Recall of IV Extension Sets with BD Q-Syte[TM] Luer Access Device
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Indication for Crestor
  • From: U.S. Food & Drug Administration (FDA)
• FDA Unveils Initiative to Reduce Unnecessary Radiation Exposure from Medical Imaging
  • From: U.S. Food & Drug Administration (FDA)
• BD Announces Worldwide Voluntary Recall ofBD Q-Syte[TM] Luer Access Devices and BD Nexiva[TM] Closed IV Catheter Systems
  • From: U.S. Food & Drug Administration (FDA)
• Turkey Hill Dairy Issues Recall On Chocolate Marshmallow Ice Cream That May Contain Undeclared Treenuts (Almonds)
  • From: U.S. Food & Drug Administration (FDA)
• Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- Questions and Answers for Healthcare Professionals: CRESTOR and the JUPITER Trial
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Guidance to Help Streamline Medical Device Clinical Trials
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Drug Safety Communication: Risk of Progressive Multifocal Leukoencephalopathy (PML) for the use of Tysabri
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tysabri (Natalizumab): Risk of developing progressive multifocal leukoencephalopathy (PML) increases with increasing duration of exposure to Tysabri
  • From: FDA MedWatch
• Cousins Products, Llc, Issues An Allergy Alert On Undeclared Egg, Soy, And Wheat In Spinach Vinaigrette
  • From: U.S. Food & Drug Administration (FDA)
• Haifa Smoked Fish Inc. Issues An Allert On Uneviscerated Whole Schmaltz Herring
  • From: U.S. Food & Drug Administration (FDA)
• Safesheath CSG Coronary Sinus Guide Hemostatic Introducer System: Class 1 Recall -Sheath tip may break off and separate while the sheath is inside blood vessel
  • From: FDA MedWatch
• FDA Updates Statement on the Investigation into the Salmonella Montevideo Outbreak
  • From: U.S. Food & Drug Administration (FDA)
• Pierino Frozen Foods Inc. Issues an Allergy Alert on Undeclared Eggs in Its Jumbo Shells with Cheese
  • From: U.S. Food & Drug Administration (FDA)
• United States Seizes more than 1500 Cases of Food from Wisconsin Distribution Warehouse
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 3, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2010 FDA Patient Safety News now available
  • From: FDA MedWatch
• FDA's MedWatch Safety Alerts: January 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves Xiaflex for Debilitating Hand Condition
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Xiaflex for Debilitating Hand Condition
  • From: U.S. Food & Drug Administration (FDA)
• Global Commodities Inc. Issues Allergy Alert On Undeclared Sulfites In Aahu Barah Brand Dry Apricot
  • From: U.S. Food & Drug Administration (FDA)
• FDA Requests $4.03 Billion to Transform Food Safety System, Invest in Medical Product Safety, Regulatory Science
  • From: U.S. Food & Drug Administration (FDA)
• FDA Announces Safety Risk Associated with HIV Drug
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Expands Use of Approved Breast Cancer Drug
  • From: U.S. Food & Drug Administration (FDA)
• FDA Statement on the Investigation into the Salmonella Montevideo Outbreak
  • From: U.S. Food & Drug Administration (FDA)
• FDA Expands Use of Approved Breast Cancer Drug
  • From: U.S. Food & Drug Administration (FDA)
• Zyprexa (olanzapine): Use in Adolescents - Clinicians should consider potential long-term risks when prescribing to adolescents
  • From: FDA MedWatch
• Eat for a Healthy Heart
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Stakeholder Advisory: FDA Technical Briefing on Its FY 2011 Budget Request
  • From: U.S. Food & Drug Administration (FDA)
• Videx/Videx EC (didanosine): Labeling Revision - Risk of Non-Cirrhotic Portal Hypertension
  • From: FDA MedWatch
• United States Seizes Unapproved Ozone Generators
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Serious Liver Disorder Associated with the Use of Videx/Videx EC (didanosine)
  • From: U.S. Food & Drug Administration (FDA)
• Edwards Lifesciences Aquarius Hemodialysis System: Recall
  • From: U.S. Food & Drug Administration (FDA)
• Hettich Centrifuges with 2050 and 2076 Plastic Rotors: Recall
  • From: U.S. Food & Drug Administration (FDA)
• Edwards Lifesciences Aquarius Hemodialysis System: Recall - Clinically significant fluid imbalance and potential for users to repeatedly override the fluid imbalance alarm
  • From: FDA MedWatch
• Hettich Centrifuges with Plastic Rotors: Recall - Hematocrit rotor may crack, break apart and be forcefully ejected
  • From: FDA MedWatch
• Drug Information Update - FDA Issues a Draft Guidance for Industry on Assessment of Abuse Potential of Drugs
  • From: U.S. Food & Drug Administration (FDA)
• Infusion Set Needles [Manufactured by Nipro for Exelint]: Recall
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Upcoming Veterinary Medicine Advisory Committee Meeting to Discuss ProHeart® 6
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 27, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA Announces Class I Recall of Certain Infusion Set Needles
  • From: U.S. Food & Drug Administration (FDA)
• Velcade (bortezomib): Starting Dose Adjustments-Patients with moderate/severe hepatic impairment should be treated with reduced starting doses, closely monitored
  • From: FDA MedWatch
• Infusion Set Needles [Manufactured by Nipro for Exelint]: Class I recall due to "coring", dislodging of silicone cores/slivers from ports into which inserted
  • From: FDA MedWatch
• FDA Announces Class I Recall of Certain Infusion Set Needles
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Morphine Sulfate Oral Solution for Relief of Acute and Chronic Pain
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Morphine Sulfate Oral Solution for Relief of Acute and Chronic Pain
  • From: U.S. Food & Drug Administration (FDA)
• FDA 101: Smoking Cessation Products
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA approves Victoza (liraglutide) to treat type 2 diabetes mellitus in adults
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves New Treatment for Type 2 Diabetes
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Percutaneous Heart Valve
  • From: U.S. Food & Drug Administration (FDA)
• Warning: Counterfeit Alli
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Ampyra to Improve Walking in Adults with Multiple Sclerosis
  • From: U.S. Food & Drug Administration (FDA)
• Nipro Medical Corporation Issues a Voluntary Recall of All GlucoPro Insulin Syringes
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Ampyra to Improve Walking in Adults with Multiple Sclerosis
  • From: U.S. Food & Drug Administration (FDA)
• Hettich Centrifuges Issues a North America and Canada Recall of Plastic Hematocrit Rotors
  • From: U.S. Food & Drug Administration (FDA)
• FDA Schedules Public Meeting on Premarket Clearance Process for Medical Devices
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- UPDATED Public Health Alert: Counterfeit Alli containing sibutramine
  • From: U.S. Food & Drug Administration (FDA)
• UPDATE - Alli 60 mg capsules : Counterfeit Product containing undeclared drug, sibutramine, in up to 3 times usual daily dose
  • From: FDA MedWatch
• Nipro GlucoPro Insulin Syringes: Recall - Needles may become detached and remain in the skin
  • From: FDA MedWatch
• The Wisconsin Cheeseman® Recalls Cheese Logs/Cheese Balls
  • From: U.S. Food & Drug Administration (FDA)
• Meridia (sibutramine hydrochloride): New contraindication to use in patients with history of CV disease
  • From: FDA MedWatch
• Drug Information Update- Follow-Up to the November 2009 Early Communication about an Ongoing Safety Review of Sibutramine, Marketed as Meridia
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Warns Consumers about Counterfeit Alli
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves Left Ventricular Assist System for Severe Heart Failure Patients
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 20, 2010
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Bellevue, Washington Salon Owner Sentenced in Connection with Unlicensed Cosmetic Treatments
  • From: U.S. Food & Drug Administration (FDA)
• Alli 60 mg capsules: Counterfeit Product - sold on Internet and containing undeclared drug, sibutramine
  • From: FDA MedWatch
• FDA Warns Consumers about Counterfeit Alli
  • From: U.S. Food & Drug Administration (FDA)
• Hines Nut Company Announces Recall of Pine Nuts Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• PEO Chapter FO Recalls Roasted Hazelnuts Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• MuscleMaster.com Conducts a Voluntary Nationwide Recall of Certain Body Building Products
  • From: U.S. Food & Drug Administration (FDA)
• FDA Commissioner Addresses Nation's Health Care Professionals on H1N1 Vaccine Safety
  • From: U.S. Food & Drug Administration (FDA)
• Parkers Farm, Inc. Expands Recall to Include All of Its Products, Regardless of Code Dates, Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 13, 2010
  • From: U.S. Food & Drug Administration (FDA)
• MuscleMaster(dot)com products: Recall (Corrected link provided for previous notification)
  • From: FDA MedWatch
• MuscleMaster.com products: Recall - Sold as dietary supplements but containing undeclared steroid drug product
  • From: FDA MedWatch
• FDA MedWatch - Dear Healthcare Professional Letter re: H1N1 vaccine safety from FDA Commissioner Hamburg
  • From: FDA MedWatch
• McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the Americas, UAE, and Fiji
  • From: U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare OTC products: Recall - 12/09 recall of Tylenol arthritis caplets now expanded to multiple other products
  • From: FDA MedWatch
• Drug Information Update: McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New -- FDA Basics
  • From: U.S. Food & Drug Administration (FDA)
• FDA Health Alert for Merrick Beef Filet Squares Dog Treats Packaged and Distributed by Merrick Pet Care
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Anesthesiologist Charged With Falsifying Medical Research
  • From: U.S. Food & Drug Administration (FDA)
• FDA Health Alert for Merrick Beef Filet Squares Dog Treats Packaged and Distributed by Merrick Pet Care
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Updates Earlier Guidance on Respiratory Treatment Spiriva HandiHaler
  • From: U.S. Food & Drug Administration (FDA)
• FDA Updates Earlier Guidance on Respiratory Treatment Spiriva HandiHaler
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Longmont, Colorado Man Arrested For Removing And Replacing Labels On Gatorade Bottles
  • From: U.S. Food & Drug Administration (FDA)
• HAPPYTOT Stage 4 and HAPPYBABY Stage 1 & Stage 2 Pouch Meals - Recall
  • From: U.S. Food & Drug Administration (FDA)
• Nurture, Inc. Issues Voluntary Recall on select HAPPYTOT Stage 4 and HAPPYBABY Stage 1 & Stage 2 Pouch Meals Due to a Packaging Defect that could cause a Possible Bacterial Contamination
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Consumer Alert on HAPPYTOT Stage 4 and Some HAPPYBABY Stage 1 & Stage 2 Baby Foods
  • From: U.S. Food & Drug Administration (FDA)
• FDA Issues Consumer Alert on HAPPYTOT Stage 4 and Some HAPPYBABY Stage 1 & Stage 2 Baby Foods
  • From: U.S. Food & Drug Administration (FDA)
• HAPPYTOT and HAPPYBABY Pouch Meals - Recall due to packaging defect that could cause possible bacterial contamination
  • From: FDA MedWatch
• Heluva Good Recalls Cold Pack Cheese Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Parkers Farm, Inc. Recalls Several Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Launches "FDA Basics" Online to Enhance Public Understanding of the Agency
  • From: U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: December 2009
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Unveils First Phase of Transparency Initiative
  • From: U.S. Food & Drug Administration (FDA)
• FDA Unveils First Phase of Transparency Initiative
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves New Drug for Rheumatoid Arthritis
  • From: U.S. Food & Drug Administration (FDA)
• Rudolph Foods Issues Allergy Alert on Undeclared Milk in Product
  • From: U.S. Food & Drug Administration (FDA)
• PARKERS FARM, INC. RECALLS SEVERAL PRODUCTS BECAUSE OF POSSIBLE HEALTH RISK
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - December 2009 Drug Safety Labeling Changes: 28 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• Rapamune (sirolimus): Drug Monitoring Recommendations-Switching between assays for the same patient can produce differing results that may be clinically significant
  • From: FDA MedWatch
• FDA Approves New Drug for Rheumatoid Arthritis
  • From: U.S. Food & Drug Administration (FDA)
• FDA Requires Sybaritic, Inc. to Stop Producing Unapproved Medical Devices
  • From: U.S. Food & Drug Administration (FDA)
• FDA Awards Contract to Harvard Pilgrim to Develop Pilot for Safety Monitoring System
  • From: U.S. Food & Drug Administration (FDA)
• FDA Ends Maryland Seafood Processor's Pattern of Sanitary Violations
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces the Availability of the 4th Edition of the Animal Feed Safety System Framework Document
  • From: U.S. Food & Drug Administration (FDA)
• Bao Ding Seafood Recalls Boiled Horse Mackerel
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2010 FDA Patient Safety News now available
  • From: FDA MedWatch
• FDA Seizes More Than $1 Million Worth of Food from Nashville Food Processor and Warehouse: Agency acts to prevent distribution of food from rodent-infested facility
  • From: U.S. Food & Drug Administration (FDA)
• ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 6, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Harry London Candies, Inc. announces a voluntary and limited recall of Harry London Chocolate Pecan Caramel Stars due to an undeclared allergen
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ev3 Endovascular Inc. Trailblazer Support Catheter: Device may crack near the radiopaque marker band, potentially resulting in serious patient injury
  • From: FDA MedWatch
• FDA Takes Action Against New Jersey Cheese Manufacturer
  • From: U.S. Food & Drug Administration (FDA)
• Nutty Guys Issues Public Notice on Voluntary Recall of Butter Toffee Peanuts and Yogurt Covered Peanuts
  • From: U.S. Food & Drug Administration (FDA)
• Nzu, Traditional Remedy for Morning Sickness:Women advised to avoid because of potential health risks from high levels of lead and arsenic
  • From: FDA MedWatch
• Publix Issues Allergy Alert on Pecans in Publix Pumpkin Pecan Streusel Pie
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA, Health Organizations to Study Safety of Medications Taken During Pregnancy
  • From: U.S. Food & Drug Administration (FDA)
• FDA, Health Organizations to Study Safety of Medications Taken During Pregnancy
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 30, 2009
  • From: U.S. Food & Drug Administration (FDA)
• Janzen Farms Recalls Hazelnut Kernels Because of Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Colorado-Based Spectranetics Corporation to Pay $5 Million to Resolve Allegations Relating to Its Medical Devices
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns Public of Continued Extortion Scam by FDA Impersonators
  • From: U.S. Food & Drug Administration (FDA)
• Tylenol Arthritis Pain Caplet 100 count: Recall of all lots due to reports of odor associated with nausea, vomiting and diarrhea
  • From: FDA MedWatch
• Mcneil Consumer Healthcare Announces A Voluntary Nationwide Recall Of All Lots Of Tylenol® Arthritis Pain 100 Count With Ez-Open Cap
  • From: U.S. Food & Drug Administration (FDA)
• Encompass Group Voluntarily Recalls Thermoflect Product Line
  • From: U.S. Food & Drug Administration (FDA)
• Thermoflect Blankets and product line - Recall: Products are not to be used in MR environment
  • From: FDA MedWatch
• Mountain Man Nut & Fruit Co.® Announces Voluntary Recall of Hazelnut
  • From: U.S. Food & Drug Administration (FDA)
• Market of Choice Recalls Hazelnuts Because of Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves A High Dose Seasonal Influenza Vaccine Specifically Intended for People Ages 65 and Older
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Orphan Drug Workshops Scheduled For Feb. 25-26 and Aug. 3-4, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Burnt Ridge Orchards, Inc. Recalls Shelled Hazelnuts Because of Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update: Follow-Up to the August 2008 Early Communication About an Ongoing Safety Review of Ezetimibe/Simvastatin, Simvastatin and Ezetimibe
  • From: U.S. Food & Drug Administration (FDA)
• Health Fraud Awareness (video)
  • From: U.S. Food & Drug Administration (FDA)
• Teva Animal Health, Inc. expands a voluntary nationwide recall of Ketamine Hydrochloride Injection, USP CIII 100mg/mL in 10mL vials
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market® Recalls Bulk Hazelnuts
  • From: U.S. Food & Drug Administration (FDA)
• Harry and David Conducts Hazelnut Recall in Medford, Oregon because of Possible Risk to Health
  • From: U.S. Food & Drug Administration (FDA)
• Evonuk Oregon Hazelnuts Recalls Raw and Dry Roasted Hazelnut Kernels Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Kunze Farms Recalls Hazelnut Kernels because of Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 16, 2009
  • From: U.S. Food & Drug Administration (FDA)
• Willamette Shelling Recalls Shelled Hazelnuts Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Willamette Filbert Growers Recalls Shelled Hazelnuts and Shelled Organic Hazelnus Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Faribault Foods Voluntarily Recalls Three Lots of Health Valley Organic No Salt Added Split Pea Soup Due to the Presence of an Undeclared Allergen
  • From: U.S. Food & Drug Administration (FDA)
• Cleviprex (clevidipine butyrate): Recall of injectable emulsion due to presence of particulate matter
  • From: FDA MedWatch
• The Medicines Company Issues a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2009 Drug Safety Labeling Changes: 44 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• FDA Approves Generic Aricept to Treat Dementia Related to Alzheimer's Disease
  • From: U.S. Food & Drug Administration (FDA)
• Atlas Operations: Recall of Sexual Enhancement Products - Undeclared drug, sulfoaildenafil, may result in lowering blood pressure to dangerous levels
  • From: FDA MedWatch
• Drug Information Update- FDA Approves First Generic Aricept to Treat Dementia Related to Alzheimer's Disease
  • From: U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Aricept to Treat Dementia Related to Alzheimer's Disease
  • From: U.S. Food & Drug Administration (FDA)
• FDA Expands Presence Outside U.S. with Opening of Mexico City Post
  • From: U.S. Food & Drug Administration (FDA)
• Simple Foods, Inc. - Undeclared allergen (milk)
  • From: U.S. Food & Drug Administration (FDA)
• Atlas Operations, Inc. Issues a Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Drug Information Update - Public Health Advisory: Availability of Tamiflu for Oral Suspension
  • From: U.S. Food & Drug Administration (FDA)
• Limited Recall of 120 Cartons of Berries & Balsamic Salad due to Unlabeled Allergen
  • From: U.S. Food & Drug Administration (FDA)
• FDA Debars Convicted Virginia Seafood Dealer from Importing Food for 20 Years
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Notice of Pilot Project of Electronic Margin of Safety and Submission of NonClinical Toxicology Study Data
  • From: U.S. Food & Drug Administration (FDA)
• Pet Carousel Conducts Nationwide Recall of Beef Hoof Products and Pig Ears Because of Salmonella Risk
  • From: U.S. Food & Drug Administration (FDA)
• Negative Pressure Wound Devices Draw FDA Notice, Advice
  • From: U.S. Food & Drug Administration (FDA)