FDA News

• Thread Index

• FDA MedWatch - Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall - Software Defect May Cancel Shock
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Consumers warned to avoid eating oysters from area 1642 in Apalachicola Bay, Florida
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Multi-Mex Distributor Inc. Dietary Supplements: Recall - Product Packaging Mimics OTC Antibiotics
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Multi-Mex Distributor Inc. Announces Recall of Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Produce N.A. Inc. Voluntarily Recalls Grape Tomatoes Grown by Six L's Packing Due to Potential Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Grape Tomatoes Distributed to Albertsons, Raley’s, Safeway, Savemart, Sam’s Club, & Walmart
  • From: FoodSafety.gov
• Allergy Alert: Walnuts In GFS Pecan Pieces
  • From: FoodSafety.gov
• Allergy Alert: Better Batter Mixes
  • From: FoodSafety.gov
• Allergy Alert: English Muffins and Bread
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Allergy Alert: J. Gumbo's Chicken Products
  • From: FoodSafety.gov
• Allergy Alert: Barbecue Beef, Pork and Chicken Products
  • From: FoodSafety.gov
• Ralcorp Frozen Bakery Products Issues Voluntary Allergen Recall of Market Pantry
  • From: FoodSafety.gov
• RECALL: Grape Tomatoes
  • From: FoodSafety.gov
• Northeast Produce Inc. Recalls Grape Tomatoes Due to Salmonella Risk associated with Six L's Packing Company Inc. in Immokalee, FL
  • From: U.S. Food & Drug Administration (FDA)
• Ralcorp Frozen Bakery Products Issues Voluntary Allergen Recall of Market Pantry
  • From: U.S. Food & Drug Administration (FDA)
• Dear Abby features Healthy Moms Advice Kit for Women's Health Week
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Needleless Pre-filled Glass Syringes: Drug Safety Communication - Compatibility Problems with Needleless Intravenous Access Systems
  • From: FDA MedWatch
• Nut Bar Company Issues Allergy Alert On Undeclared Walnuts In GFS Pecan Pieces
  • From: U.S. Food & Drug Administration (FDA)
• Flowers Foods Issues Voluntary Recall on Certain English Muffins and One Bread Item
  • From: U.S. Food & Drug Administration (FDA)
• TRI-STATE Baking Company, L.L.C. Issues Allergy Alert On Undeclared Soy Flour, Soy Lecithin, And/Or Milk In Product
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Caffeine & Sodium Benzoate Injection, USP 250 mg/mL, 2 mL Single Dose Vial Due to Visible Particulates
  • From: U.S. Food & Drug Administration (FDA)
• Taylor Farms Pacific, Inc. Recalls Grape Tomatoes Due to Salmonella Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA clears first test to quickly diagnose and distinguish MRSA and MSSA
  • From: U.S. Food & Drug Administration (FDA)
• FDA expands approved use for carotid stent
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Weck Hem-o-Lok Ligating Clips: Contraindicated for Ligation of Renal Artery During Laparoscopic Living-Donor Nephrectomy
  • From: FDA MedWatch
• FDA approves new treatment for rare type of pancreatic cancer
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Pig Ears for Pet Treats (Possible Salmonella)
  • From: FoodSafety.gov
• ALLERGY ALERT: Portobello Mushroom Flavored Pork Loins Contain Whey (Milk)
  • From: FoodSafety.gov
• RECALL: Grape Tomatoes
  • From: FoodSafety.gov
• Mastronardi Produce Voluntarily Recalls Grape Tomatoes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Safeway Recalls Kabobs Made with Grape Tomatoes in Several States
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 4, 2011
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New- FDA issues first new rules under Food Safety Modernization Act
  • From: U.S. Food & Drug Administration (FDA)
• FDA issues final guidance for liquid OTC drug products with dispensing devices
  • From: U.S. Food & Drug Administration (FDA)
• FDA issues first new rules under Food Safety Modernization Act
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Keys Manufacturing Company, Inc. Recalls Pig Ears for Pet Treats Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Keys Manufacturing Company, Inc. Recalls Pig Ears for Pet Treats Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• New Features on FDA Office of Women's Health Website
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces the Availability of the NARMS 2008 Executive Report
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Boston Scientific Devices Stolen - Risk of Infection
  • From: FDA MedWatch
• FDA, FTC act to remove fraudulent STD products from the market
  • From: U.S. Food & Drug Administration (FDA)
• Defibtech Announces a Voluntary Recall of DDU-100 series AEDs
  • From: U.S. Food & Drug Administration (FDA)
• Taylor Farms Pacific, Inc. Recalls Grape Tomatoes Due to Salmonella
  • From: U.S. Food & Drug Administration (FDA)
• Six L's Voluntarily Recalls Grape Tomatoes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (Warfarin Sodium) Crystalline 5 mg Tablets, Lot Number 9H49374A
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Coumadin (warfarin sodium) Crystalline 5 mg Tablets: Recall - Tablets May Have Higher than Expected Potency
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - NARMS 2008 Executive Report Now Available
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for Type 2 diabetes
  • From: U.S. Food & Drug Administration (FDA)
• The May 2011 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Quinault Tribal Enterprise Recalls All Canned Seafood Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Organic Food Bar, Inc. Expands its Voluntary Recall on Chocolatey Chocolate Chip Bars to Include Additional Products and Lots
  • From: U.S. Food & Drug Administration (FDA)
• Satur Farms, LLC Recalls Satur Farms Cilantro Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Issue of FDA Veterinarian
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Update to Fuzeon (enfuvirtide) label regarding incidence of bacterial pneumonia
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 27, 2011
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Elise Grace's Dip and Soup Mixes
  • From: FoodSafety.gov
• ALLERGY ALERT: Better Batter Mixes
  • From: FoodSafety.gov
• American Regent Initiates Voluntary Nationwide Recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10 mL) 10 mL Single Dose Vial Due to the Presence of Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• The Raymond-Hadley Corporation Issues Allergy Alert on Undeclared Milk in Better Batter Brand 20oz. & 2.5lb. Pancake & Biscuit Mix, 18.25oz. Yellow Cake Mix, and 18.25oz. Chocolate Cake Mix
  • From: U.S. Food & Drug Administration (FDA)
• Elise Grace's Dry Food Company Issues Nationwide Allergy Alert Because Of Undeclared Allergens In Their Dry Food Products Line
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA Antiviral Advisory Committee April 28, 2011 meeting background materials available: telaprevir for Hepatitis C
  • From: U.S. Food & Drug Administration (FDA)
• Woodsmoke Provisions Voluntarily Recalls 160 packages of 4 oz. The Fresh Market Signature Collection Atlantic Smoked Salmon Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• L&M Companies, Inc. Recalls One Lot of Whole Cucumbers Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Important Information for Atwater Carey First Aid Kit Consumers Regarding Triad Group's Povidone Iodine Prep Pads
  • From: U.S. Food & Drug Administration (FDA)
• Jonathans Sprouts Recalls Alfalfa Sprouts Because of Possible Health Risk Extends Recall of 4/19/11 to Additional Products and Codes )
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Doctor's CarbRite Chocolate Brownie Diet Bars
  • From: FoodSafety.gov
• RECALL: The Fresh Market Signature Collection Atlantic Smoked Salmon
  • From: FoodSafety.gov
• ALLERGY ALERT: Carob Brown Rice Crunch Squares & Carob Mint Miniatures
  • From: FoodSafety.gov
• RECALL: Whole Cucumbers
  • From: FoodSafety.gov
• RECALL: Jonathans Alfalfa Sprouts
  • From: FoodSafety.gov
• FDA Hepatitis Update - April 27, 2011 FDA Advisory Committee background materials available: boceprevir for Hep C
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves the first vaccine to prevent meningococcal disease in infants and toddlers
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves the first vaccine to prevent meningococcal disease in infants and toddlers
  • From: U.S. Food & Drug Administration (FDA)
• Satur Farms, LLC Recalls Satur Farms Cilantro Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Doctor's CarbRite Diet Issues Allergy Alert on Certain Chocolate Brownie Flavored Bars
  • From: U.S. Food & Drug Administration (FDA)
• MedWatch - Safety update on Progressive Multifocal Leukoencephalopathy (PML) associated with Tysabri (natalizumab)
  • From: FDA MedWatch
• Update of CVM's What's New - April 2011 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Summersweet seafood mouses and dips, possible Listeria
  • From: FoodSafety.gov
• RECAL: Alfalfa Sprouts
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Jonathans Sprouts Recalls Alfalfa Sprouts Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA warns companies to stop making MRSA claims for over-the-counter products
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Rituxan to treat two rare disorders
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• B&M, Inc. Conducts Voluntary Nationwide Recall Of 6 Lot Numbers Of Archer Farms Ground Turmeric Due To Excessive Lead Levels.
  • From: U.S. Food & Drug Administration (FDA)
• Organic Food Bar, Inc. Issues Allergy Alert on Chocolatey Chocolate Chip Raw Organic Food Bars
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Archer Farms Ground Turmeric Sold at Target
  • From: FoodSafety.gov
• ALLERGY ALERT: Chocolate Chip Organic Food Bars
  • From: FoodSafety.gov
• FDA approves new medical device for form of brain cancer
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Actemra to treat rare form of juvenile arthritis
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 13, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lansoprazole Delayed-Release Orally Disintegrating Tablets by Teva Pharmaceuticals: Letter to Healthcare Professionals - Clogged, Blocked Oral Syringes and Feeding Tubes
  • From: FDA MedWatch
• Ortho-McNeil Neurologics Voluntarily Recalls Two Lots of TOPAMAX®
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Topamax (topiramate): Recall - Musty Odor
  • From: FDA MedWatch
• Drug Shortages Update
  • 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 - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tumor Necrosis Factor (TNF) blockers, Azathioprine and/or Mercaptopurine: Update on Reports of Hepatosplenic T-Cell Lymphoma in Adolescents and Young Adults
  • From: FDA MedWatch
• FDA MedWatch - Penumbra Coil 400 by Penumbra Inc.: Class 1 Recall - Premature Detachment of the Coil
  • From: FDA MedWatch
• FDA MedWatch - Axxent FlexiShield Mini by iCAD (formerly Xoft Inc.): Recall - Product May Shed Particles of Tungsten
  • From: FDA MedWatch
• FDA approves new treatment for large brain aneurysms
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Shortage Information and Notice of FSMA Public Meeting
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• March 2011 Safety Labeling Changes: 55 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Mexicantown Whole Issues Allergy Alert On Undeclared Pecans In Pan Nuez And Undeclared Milk In Magdalena, Pan De Maiz, YoyoPan Nuez, And Tacos De Pan Danes
  • From: U.S. Food & Drug Administration (FDA)
• Moog Recalls Curlin Ambulatory Infusion Pump Models 6000 CMS, 6000 CMS IOD, PainSmart, and PainSmart IOD
  • From: U.S. Food & Drug Administration (FDA)
• Waco's Bestyett Sandwiches issues a Voluntary Recall of Pimento Cheese Sandwiches and Chicken Salad Sandwiches due to Undeclared EGGS
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Revlimid (lenalidomide): Ongoing Safety Review - increased risk of developing new malignancies
  • From: FDA MedWatch
• RECALL: Smoked Salmon
  • From: FoodSafety.gov
• ALLERGY ALERT: Le Bon Patissier Products
  • From: FoodSafety.gov
• ALLERGY ALERT: Chicken of the Sea Chopped Clams May Contain Shrimp
  • From: FoodSafety.gov
• RECALL: Spinach
  • From: FoodSafety.gov
• FDA clears test for bacteria that can cause serious intestinal disease
  • From: U.S. Food & Drug Administration (FDA)
• Tri-Union Seafoods Issues Precautionary, Voluntary Recall Of Limited 6.5-Ounce Chopped Clams
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Horizant to treat restless legs syndrome
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Benzocaine Topical Products: Sprays, Gels and Liquids - Risk of Methemoglobinemia
  • From: FDA MedWatch
• Le Bon Patissiere-2, Inc. Announces Voluntary Recall On Select Le Bon Patissiere Products That Contain Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Fresh Express Announces Precautionary Recall of a Limited Number of Cases of 9 oz. Bag Spinach Due to Possible Health Risk from Salmonella
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 6, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update -
  • From: U.S. Food & Drug Administration (FDA)
• FDA acts to prevent contamination problems with Triad antiseptic products
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for rare form of thyroid cancer
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Veterinary Master Files
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - AAVPT Veterinary Drug Regulatory Life Cycle Course
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update April 26, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Yervoy (ipilimumab): Risk Evaluation and Mitigation Strategy (REMS) - Severe Immune-Mediated Adverse Reactions
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FoodSafety.gov News Update
  • From: FoodSafety.gov
• FDA Webinar on "Bad Ads" Program on April 28, 2011
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Fitness Labs and Lindberg Protein Supplements
  • From: FoodSafety.gov
• RECALL: Smoked Salmon
  • From: FoodSafety.gov
• RECALL: Jalapeno Peppers
  • From: FoodSafety.gov
• ALLERGY ALERT: Egg in Frozen Chicken Fillets
  • From: FoodSafety.gov
• RECALL: Smoked Round Scad Fish (galunggong)
  • From: FoodSafety.gov
• ALLERGY ALERG: Egg White in Cottage Grove Farmhouse Bakery Breads
  • From: FoodSafety.gov
• ALLERGY ALERT: Peanut Oil, Egg, Soy in Sassy Cow Creamery Ice Cream
  • From: FoodSafety.gov
• Update of CVM's What's New - FDA launches consumer-friendly Web search for consumers during recalls
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Frankly Fresh Seafood Products
  • From: FoodSafety.gov
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Sprouts
  • From: FoodSafety.gov
• AVNS, Inc. Issues a Voluntary Recall of THE BEST Enhancer
  • From: U.S. Food & Drug Administration (FDA)
• FDA launches consumer-friendly Web search for consumers during recalls
  • From: U.S. Food & Drug Administration (FDA)
• Cottage Grove Farmhouse Bakery Issues Allergy Alert On Undeclared Pasteurized Egg White In Breads
  • From: U.S. Food & Drug Administration (FDA)
• Centurion Medical Products Initiates Voluntary Recall of Customized Convenience Kits (including select Central Venous Catheter, PICC Insertion, and VAD Trays) that contain American Regent's Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials
  • From: U.S. Food & Drug Administration (FDA)
• Arko Foods International Recalls Angelina Brand Smoked Roundscad Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• The April 2011 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Arko Foods International Recalls Angelina Brand Smoked Roundscad Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Louie Foods International Voluntarily Recalls Certain Sprouts
  • From: U.S. Food & Drug Administration (FDA)
• Frankly Fresh Inc. Voluntarily Recalls Seafood Salad Products Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA proposes draft menu and vending machine labeling requirements, invites public to comment on proposals
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Labeling changes to Tyzeka (telbivudine) 600 mg tablets and oral solution 100 mg/5 mL reflect risk of resistance-associated substitutions
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heartstring II Proximal Seal System (HS-1045) by Maquet Cardiovascular, LLC: Recall - Insufficient Adhesive
  • From: FDA MedWatch
• FDA MedWatch - Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F by Millar Instruments Inc.: Class 1 Recall
  • From: FDA MedWatch
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• THE SMOKEHOUSE LLC RECALLS ONE BATCH OF PORTIER FINE FOODS NORWEGIAN SMOKED SALMON BECAUSE OF POSSIBLE HEALTH RISK
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Meds IV Pharmacy, IV Compounded Products Recall: Outbreak of Serratia Marcescens Bacteremia in Alabama Hospitals
  • From: FDA MedWatch
• CDC And ADPH Investigate Outbreak At Alabama Hospitals; Products Recalled
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• New Cosmetics Consumer Update and Video
  • From: U.S. Food & Drug Administration (FDA)
• Nutrition Express Voluntarily Recalls Protein Supplements Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Trader Joe's Pizza Al Pollo Asado
  • From: FoodSafety.gov
• FDA MedWatch - Pradaxa (dabigatran etexilate mesylate) Capsules: Special Storage and Handling Requirements
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of emtricitabine capsules, 200 mg
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces the Approval of Iron Dextran for Baby Pigs
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - X-Hero and Male Enhancer: Recall - Undeclared Drug Ingredient
  • From: FDA MedWatch
• FDA MedWatch - Roche ACCU-CHEK FlexLink Plus Infusion Set: Class I Recall - Potential for Under-Delivery of Insulin
  • From: FDA MedWatch
• Recall of Arnica Flower And Stem Arnica Due To Inaccurate Usage Information On Product Label
  • From: U.S. Food & Drug Administration (FDA)
• USA Far Ocean Group Inc. Issues Voluntary Nationwide Recall of X-Hero and Male Enhancer, Products Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Soladek Vitamin Solution: Unapproved Product May Contain Dangerously High Levels of Vitamins A and D
  • From: FDA MedWatch
• HIV/AIDS Update - Approval of VIRAMUNE XR (nevirapine) 400 mg extended release tablet
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Bubble Gum with Elevated Levels of Lead
  • From: FoodSafety.gov
• ALLERGY ALERT: Egg in Mai's Bakery Hopia Mongo and Moon Cake Products
  • From: FoodSafety.gov
• FDA MedWatch - Citalopram And Finasteride by Greenstone: Recall - Possible Mislabeling
  • From: FDA MedWatch
• FDA MedWatch - Irinotecan Hydrochloride Injection: Recall - Fungal Microbial Contaminant
  • From: FDA MedWatch
• Candy Dynamics Recalls Toxic Waste® Short Circuits[TM] Bubble Gum Net wt. 3.2 oz. (90g) Package --- Lot # 15070SC12
  • From: U.S. Food & Drug Administration (FDA)
• APP Pharmaceuticals Issues A Nationwide Voluntary Recall Of Irinotecan Hydrochloride Injection
  • From: U.S. Food & Drug Administration (FDA)
• Greenstone Announces Voluntary Nationwide Recall Of Citalopram And Finasteride Due to Possible Mislabeling
  • From: U.S. Food & Drug Administration (FDA)
• Mai's Bakery Issues Allergy Alert For Undeclared Eggs in Their Packages of "Hopia Mongo" and "Moon Cake" Products
  • 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 - FR Notice; Extension of Comment Period for The National Antimicrobial Resistance Monitoring System Strategic Plan 2011-2015
  • From: U.S. Food & Drug Administration (FDA)
• RECALLS: Serrano Peppers, Protein Supplements, Smoked Ham and Bacon Products, Pickled Beets, Bologna, Cantaloupes
  • From: FoodSafety.gov
• ALLERGY ALERTS: Kashi Southwest Style Chicken Products, Wheat Bread
  • From: FoodSafety.gov
• FDA approves Zostavax vaccine to prevent shingles in individuals 50 to 59 years of age
  • From: U.S. Food & Drug Administration (FDA)
• Unified Grocers Issues Allergy Alert on Undeclared Milk in Cottage Hearth Stone Ground Wheat Bread (24 oz) and 7 Select 100% Whole Wheat Bread (24 oz)
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA and the Assoc. of American Feed Control Officials collaborate on the development of Animal Feed Regulatory Program Standards
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - March 2011 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• USA Far Ocean Group, Inc. Issues Voluntary Nationwide Recall of U-Prosta, a Product Marketed As a Dietary Supplement That Contains Undeclared Terazosin Hydrochloride
  • From: U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Poduce Voluntairly Recalls Cantalopes Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 23, 2011
  • From: U.S. Food & Drug Administration (FDA)
• Millar Instruments, Inc. Issues a Recall of Millar Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Draft Guidance for Industry: Testing for Salmonella Species in Human Foods and Direct-Human-Contact Animal Foods
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - H&P Industries Povidine Iodine Prep Pads: Recall - Potential Microbial Contamination
  • From: FDA MedWatch
• Lilly Announces Important Action Regarding Recall of Alcohol Prep Pads Made by Triad Group Included in Forteo Starter Kits
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Single Dose Vials; 5 mL and 30 mL Multiple Dose Vials
  • From: U.S. Food & Drug Administration (FDA)
• H&P Industries, Inc. Issues a Voluntary Nationwide Recall of All Lots of Povidine Iodine Prep Pads Due to Potential Microbial Contamination
  • From: U.S. Food & Drug Administration (FDA)
• World Variety Produce, Inc. Recalls Serrano Peppers
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - American Regent Injectable Products: Recall - Visible Particulates in Products (UPDATE)
  • From: FDA MedWatch
• FDA MedWatch - Gen-Probe Inc., AccuProbe Group B Streptococcus Culture Identification Test, AccuProbe Mycobacterium Tuberculosis Complex Culture Identification Test and, AccuProbe Mycobacterium Avium Complex Culture Identification Test: Class I Recall
  • From: FDA MedWatch
• New FDA Basics Question: Is the U.S. really slower than Europe in approving new drugs?
  • From: U.S. Food & Drug Administration (FDA)
• New FDA Basics Question: Is it true FDA is approving fewer new drugs lately?
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 16, 2011
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Concentrated Sodium Chloride Injection, USP, 23.4% 30 mL Single Dose Vials and 100 mL Pharmacy Bulk Packs
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Herring and Sprats
  • From: FoodSafety.gov
• Update of CVM's What's New - Veterinary Laboratory Response Network
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated GRAS Notices Inventory and Updated Listing of Approved Medicated Feed Mill Licenses
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA Advisory Committee meeting to consider boceprevir and telaprevir, April 27 and April 28, 2011
  • From: U.S. Food & Drug Administration (FDA)
• February 2011 Safety Labeling Changes: 53 Medical Product Labels with changes to Prescribing Information
  • From: FDA MedWatch
• RECALL: Lean Cuisine Spaghetti with Meatballs
  • From: FoodSafety.gov
• RECALL: Organic Garbanzo Beans
  • From: FoodSafety.gov
• RECALL: Frozen pb jamwich from Giant-Carlisle Stores
  • From: FoodSafety.gov
• PIERRE FOODS Voluntarily Recalls 320 Cases Of Pierre TM pb jamwich, LOT 0068035 From Giant-Carlisle Stores IN MD, PA, VA AND WV
  • From: U.S. Food & Drug Administration (FDA)
• Faribault Foods Announces Voluntary Recall of Field Day Organic Garbanzo Beans Due to Mislabeling and Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Is there lead in lipstick?
  • From: U.S. Food & Drug Administration (FDA)
• Does FDA approve the color additives used in cosmetics? If so, how does FDA determine their safety?
  • From: U.S. Food & Drug Administration (FDA)
• Are henna tattoos safe?
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Beef Sticks
  • From: FoodSafety.gov
• ALLERGY ALERT: Turkey Stick Products
  • From: FoodSafety.gov
• RECALL: Chocolate Milk
  • From: FoodSafety.gov
• RECALL: Coconut Water
  • From: FoodSafety.gov
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• ONE World Enterprises Recalls O.N.E. Coconut Water Due To Mold
  • From: U.S. Food & Drug Administration (FDA)
• Oak Farms Dairy in Waco Conducts Voluntary Limited Recall of Half Gallon Plastic Bottles of Whole Chocolate Milk, Half Pint Paper Cartons of Whole Chocolate Milk, and Half Pint Paper Cartons of 1% Chocolate Milk Due to Presence of Alkaline Phosphatase in Samples
  • From: U.S. Food & Drug Administration (FDA)
• Vitalabs, Inc. Issues Voluntary Recall for Specific Lots of Whey Protein Isolate
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Pig Ear Dog Chews
  • From: FoodSafety.gov
• RECALLS: Organic Herbal Tea
  • From: FoodSafety.gov
• RECALL: Bologna
  • From: FoodSafety.gov
• CVM Updates - FDA Releases Electronic Submission Tool, eSubmitter, for Use by the Animal Health Industry
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA to Convene Public Hearing on Ensuring the Safety of Imported Foods and Animal Feed
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Draft Guidance Available
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA, Justice Department take action against McNeil-PPC Inc.
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Advises Veterinarians of Recent Recall of Human Drug, Phenobarbitol
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 9, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Benlysta to treat lupus
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Benlysta to treat lupus--First new lupus drug approved in 56 years
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval for Lamivudine and Tenofovir DF Fixed Dose Combination Tablets, 300 mg/300 mg
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Ground Beef
  • From: FoodSafety.gov
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• REMEDYTEAS Voluntarily Recalls Peppermint Organic Herbal Tea And Organic Herbal Tea Blend Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Webinar on Tattoos and Permanent Makeup
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Kaletra (lopinavir/ritonavir): Label Change - Serious Health Problems in Premature Babies
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• McCormick & Company Recalls Golden Dipt® Tempura Seafood Batter Mix Due To Unlabeled Milk Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Golden Dipt Tempura Seafood Batter Mix
  • From: FoodSafety.gov
• Unilever Announces Recall of Skippy® Reduced Fat Peanut Butter Spread Due to Possible Health Risk Limited Recall of 6 Best-If-Used-By Dates
  • From: U.S. Food & Drug Administration (FDA)
• DeFranco and Sons Recall Bulk and Consumer-packaged In-shell, Hazelnut and Mixed Nut Products Containing Hazelnuts
  • From: U.S. Food & Drug Administration (FDA)
• FDA: E. coli O157:H7 cases linked to hazelnuts
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The due date for applying to CVM's 2011 Summer Intern Program "Windows to Regulatory Research" has been extended to March 18, 2011
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval for abacavir sulfate scored tablets for oral suspension, 60 mg
  • From: U.S. Food & Drug Administration (FDA)
• FDA modifies boxed warning for pulmonary arterial hypertension drug Letairis
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Topamax (topiramate): Label Change - Risk For Development of Cleft Lip and/or Cleft Palate in Newborns
  • From: FDA MedWatch
• FDA: Risk of oral birth defects in children born to mothers taking topiramate
  • From: U.S. Food & Drug Administration (FDA)
• Food Co. Recalls Products Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA expands use of banding system for weight loss
  • From: U.S. Food & Drug Administration (FDA)
• Garden of Life, LLC. Issues a Voluntary Recall of Vitamin Code Raw Vitamin C Dietary Supplement. Recall is Limited to Raw Vitamin C Only. No Other Garden of Life Products are Involved.
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Davol XenMatrix Surgical Graft: Class I Recall - Elevated Endotoxin Levels
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cook Inc., Single, Double, Triple and Five-Lumen Central Venous Catheter Trays, Single and Double Lumen PICC Peripheral Inserted Central Venous Catheter Trays Recall
  • From: FDA MedWatch
• Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 2, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA prompts removal of unapproved drugs from market
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unapproved Cough, Cold, Allergy Products: FDA Prompts Removal From Market
  • From: FDA MedWatch
• FDA MedWatch - Proton Pump Inhibitor drugs (PPIs): Drug Safety Communication - Low Magnesium Levels Can Be Associated With Long-Term Use
  • From: FDA MedWatch
• Update of CVM's What's New - The Story of the Center for Veterinary Medicine (video)
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Safety Review update of Abacavir: no statistically significant association seen between myocardial infarction and ABC
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Wellpet LLC Voluntarily Recalls Certain Lots Of Canned Cat Food
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Abacavir - Ongoing Safety Review: Possible Increased Risk of Heart Attack
  • From: FDA MedWatch
• FDA approves new drug to treat chronic obstructive pulmonary disease
  • From: U.S. Food & Drug Administration (FDA)
• E&J Brandy Announces A Nationwide Recall Of Stainless Steel Flasks Due To Possible Lead Risk
  • From: U.S. Food & Drug Administration (FDA)
• W H & GROUP, LLC. Issues An Alert On Uneviscerated Fish
  • From: U.S. Food & Drug Administration (FDA)
• The March 2011 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Edarbi to treat high blood pressure
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Negative Pressure Wound Therapy (NPWT) systems UPDATE
  • From: FDA MedWatch
• ALLERGY ALERT: Maya Dry Fruit Kachori contains peanuts
  • From: FoodSafety.gov
• ALLERGY ALERT: Nibble with Gibble's and Kay & Ray's Chips May Contain Soy
  • From: FoodSafety.gov
• RECALL: Pacific American Fish Roe Capelin, Risk of Botulism
  • From: FoodSafety.gov
• ALLERGY ALERT: Haddon House Asian Gourmet Cheese Rice Crackers
  • From: FoodSafety.gov
• Arkansas Firm Recalls Various Meat and Poultry Products Produced Without Inspection
  • From: FoodSafety.gov
• FDA: Advanced genomic test helps trace sources of foodborne illness outbreak
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Kaletra (lopinavir/ritonavir) Oral Solution label changes related to toxicity in preterm neonates
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Label change for Viracept (nelfinavir): drug-drug interaction information with warfarin
  • From: U.S. Food & Drug Administration (FDA)
• Urgent Recall on Asian Gourmet Cheese Rice Crackers Which May Contain Undeclared Milk and Undeclared Food Coloring Additives.
  • From: U.S. Food & Drug Administration (FDA)
• Svelte 30 Nutritional Consultants Issues a Voluntary Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• FDA and Georgetown University Medical Center announce partnership
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of zidovudine water-disperable tablets, 100 mg for pediatrics/adults unable to swallow tablets
  • From: U.S. Food & Drug Administration (FDA)
• Roche Insulin Delivery Systems announces recall of ACCU-CHEK® FlexLink Plus infusion sets
  • From: U.S. Food & Drug Administration (FDA)
• Consumer Alert: Undeclared Peanuts In Dry Fruit "Kachori"
  • From: U.S. Food & Drug Administration (FDA)
• FDA: U.S. Marshals seize food products at Tennessee company
  • From: U.S. Food & Drug Administration (FDA)
• Martin's Famous Pastry Shoppe, Inc. Issues Allergy Alert On Undeclared Soy Protein In Certain "Nibble With Gibble's" And Kay And Ray's Branded Products
  • From: U.S. Food & Drug Administration (FDA)
• Pacific American Fish Co. Recall Shishamo Roe Capelin 4L Due To Potential of C. Botulinum
  • From: U.S. Food & Drug Administration (FDA)
• Advanced genomic test helps trace sources of foodborne illness outbreak
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 23, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2011 Safety Labeling Changes; 43 products with revisions to Prescribing Information
  • From: FDA MedWatch
• FDA MedWatch - Extenze Tablets: Recall
  • From: FDA MedWatch
• BIOTAB NUTRACEUTICALS, INC. Issues a Voluntary Recall of Specific Lots of the Nutritional Supplement EXTENZE (Men's Regular)
  • From: U.S. Food & Drug Administration (FDA)
• FDA permits marketing of first test for most common cause of gastroenteritis outbreaks
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
  • From: U.S. Food & Drug Administration (FDA)
• Natural Choice Distribution Company Inc. Voluntarily Recalls Certain Lots Of Fare And Square Sandwiches, Superfresh Sandwiches, And Real Wraps Burritos Due To The Presence Of Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• PHOTO - Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish
  • From: U.S. Food & Drug Administration (FDA)
• Upsher-Smith Laboratories Announces Expansion of Voluntary Nationwide Recall. Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven® and Oxybutynin
  • From: U.S. Food & Drug Administration (FDA)
• Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Antipsychotic Drugs: Class Labeling Change - Treatment During Pregnancy and Potential Risk to Newborns
  • From: FDA MedWatch
• Safety is NO Accident...National Public Health Week April 4-10, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves product to prevent bleeding in people with rare genetic defect
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Notice of Extension of Comment Period; Unapproved Animal Drugs
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Warfarin Sodium Tablets (Jantoven), 3mg: Recall - Mislabeled Bottles Containing Higher Dosage
  • From: FDA MedWatch
• FDA warns against certain uses of asthma drug terbutaline for preterm labor
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Terbutaline: Label Change - Warnings Against Use for Treatment of Preterm Labor
  • From: FDA MedWatch
• HIV/AIDS Update - Tentative approval of abacavir sulfate Oral Solution, 20 mg/mL
  • From: U.S. Food & Drug Administration (FDA)
• Upsher-Smith Laboratories Announces The Voluntary Nationwide Recall Of Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 16, 2011
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize Auralgan Otic Solution
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic SynchroMed II and SynchroMed EL Implantable Infusion Pump and Refill Kits: Class 1 Recall
  • From: FDA MedWatch
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Prime Choice Foods Corporation Voluntarily Recalls Certain Lots Of Garden Of Eatin'® Multi Grain Tortilla Chips Due To The Presence Of Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Triad Sterile Lubricating Jelly: Recall - Product May Not Be Sterile
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA seeks to invest in foodborne illness prevention, medical product safety and countermeasures
  • From: U.S. Food & Drug Administration (FDA)
• FDA finalizes regulation for certain software, hardware used with medical devices
  • From: U.S. Food & Drug Administration (FDA)
• January
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT EXPANDED: f'realStrawberry Banana Smoothies -- May Contain Peanuts
  • From: FoodSafety.gov
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
  • From: U.S. Food & Drug Administration (FDA)
• f'real® foods Expands Voluntary Recall Of Strawberry Banana Smoothies Due To Potential Peanut Content
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Barbecue Pork Sold in AL, GA, TN, MS, may contain dairy (whey)
  • From: FoodSafety.gov
• ALLERGY ALERT: Essentials, RightFood, other BioSan dietary supplements, may contain soy
  • From: FoodSafety.gov
• ALLERGY ALERT: H-E-B Frozen Breaded Okra Sold in Texas, may contain dairy (whey)
  • From: FoodSafety.gov
• RECALL: Smoked Salmon sold at The Fresh Market, possible Listeria
  • From: FoodSafety.gov
• RECALL: Ground Beef Products (Possible E. Coli Contamination)
  • From: FoodSafety.gov
• ALLERGY ALERT: f'real® Strawberry Banana Smoothies may contain peanuts
  • From: FoodSafety.gov
• ALLERGY ALERT: Frozen Yellow Fin Tuna
  • From: FoodSafety.gov
• FDA approves first 3-D mammography imaging system
  • From: U.S. Food & Drug Administration (FDA)
• f'real® foods Issues Voluntary Recall of Strawberry Banana Smoothies Due to Potential Peanut Content
  • From: U.S. Food & Drug Administration (FDA)
• FDA clears test to help patients with kidney transplants
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - February 2011 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• St James Smokehouse, Inc, Announces Voluntary Recall of Scotch Reserve Whiskey & Honey Smoked Salmon 4oz Retail Packs Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Neuro Resource Group, Inc. Informs Customers of Important Information about Triad Group's Alcohol Prep Pads
  • From: U.S. Food & Drug Administration (FDA)
• FDA Webinar on Safety of the Blood Supply
  • From: U.S. Food & Drug Administration (FDA)
• Are all personal care products regulated as cosmetics?
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 9, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arstasis One Access System: Class I Recall - Components May Fracture and/or Separate
  • From: FDA MedWatch
• Are all personal care products regulated as cosmetics?
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Letter to Veterinarians and Pharmacy Professionals re: SucroMate Equine (deslorelin acetate)
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Important information about alcohol prep pads packaged with Pegasys and certain other injection products
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Important information about alcohol prep pads packaged with Fuzeon and certain other injection products
  • From: U.S. Food & Drug Administration (FDA)
• Pandemic Influenza Evaluation and Capacity Review Tools
  • From: U.S. Dept. of Health & Human Services
• How do the activities of the USDA FSIS differ from the activities of the FDA Center for Food Safety and Applied Nutrition?
  • From: U.S. Food & Drug Administration (FDA)
• FDA launches Medical Device Innovation Initiative
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hydrocodone Bitartrate And Acetaminophen Tablets, Phenobarbital Tablets by Qualitest: Recall - Incorrect Package Labeling
  • From: FDA MedWatch
• FDA orders postmarket surveillance of certain TMJ implants
  • From: U.S. Food & Drug Administration (FDA)
• Rouses Markets Voluntarily Recalls Frozen Yellow Fin Tuna Steaks Due To Possible Health Risks
  • From: U.S. Food & Drug Administration (FDA)
• Watson Announces Important Action Related to Nationwide Recall of Triad Alcohol Prep Products Included in Products
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Potassium Phosphates Injection, USP 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium 5 mL Single Dose Vial, Lot# 0048 Due to Translucent Visible Particles
  • From: U.S. Food & Drug Administration (FDA)
• Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall Of Hydrocodone Bitartrate And Acetaminophen Tablets, USP 10 MG / 500 MG, NDC 0603-3888-20, 60 Count, Lot Numbers T150G10B, T120J10E And T023M10A And Phenobarbital Tablets, USP 32.4 MG, NDC 0603-5166-32, 1000 Count, Lot Numbers T150G10B, T
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - American Regent Injectable Products: Recall - Visible Particulates in Products
  • From: FDA MedWatch
• HIV/AIDS Update - Reyataz (atazanavir) label revised, adding dosing recommendations for pregnancy and postpartum period
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Merit Prelude Short Sheath Catheter Introducer: Class I Recall - Tip May Detach During Use
  • From: FDA MedWatch
• CVM Updates - FDA Announces Upcoming Shortage of Vetsulin for Dogs and Cats in the Critical Need Program
  • From: U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health eUpdate
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Apple Chipotle Salsa, Maple BBQ Grilling Sauce, & Pumpkin Chipotle Roasting Sauce (contain wheat)
  • From: FoodSafety.gov
• ALLERGY ALERT: Mooney's Kentucky Bourbon Cheese & Valumarket's Beer Cheese Spread (contains soy and fish)
  • From: FoodSafety.gov
• ALLERGY ALERT: Mariegold Baking White Bread and Vallarta Premium White Bread (contain milk)
  • From: FoodSafety.gov
• ALLERGY ALERT: Caesar Dressing (contains eggs)
  • From: FoodSafety.gov
• American Spoon Foods brand Apple Chipotle Salsa, Maple BBQ Grilling Sauce, and Pumpkin Chipotle Roasting Sauce may contain undeclared wheat flour and may put certain consumers at risk for wheat or gluten sensitivities or allergies.
  • From: U.S. Food & Drug Administration (FDA)
• FDA clears first diagnostic radiology application for mobile devices
  • From: U.S. Food & Drug Administration (FDA)
• Shaping Beauty, Inc. Issues a Voluntary Nationwide Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Sodium Thiosulfate Injection, USP 10% (100 mg/mL) 10 mL Single Dose Vials Lot# 0056 Due to Translucent Visible Particles
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves drug to reduce risk of preterm birth in at-risk pregnant women
  • From: U.S. Food & Drug Administration (FDA)
• FDA warns consumers not to use Fruta Planta weight loss products
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Rolf's Patisserie recalling all desserts made after November 1
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Gardasil approved to prevent anal cancer
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - UPDATE: Avandia (rosiglitazone): Information on cardiovascular risks (including heart attack) added to labeling and Medication Guide
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Updated: Undeclared Soy And Anchovy Puree In "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread"
  • From: U.S. Food & Drug Administration (FDA)
• Godi International, Corp. Issues a Voluntary Nationwide and International Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement.
  • From: U.S. Food & Drug Administration (FDA)
• Unified Grocers Issues Allergy Alert on Undeclared Milk in Mariegold Baking White Bread (24 oz) and Vallarta Premium White Bread (24 oz)
  • From: U.S. Food & Drug Administration (FDA)
• Tomaso's Issues Allergy Alert On Undeclared Eggs In Caesar Dressing
  • From: U.S. Food & Drug Administration (FDA)
• FDA reminds health care professionals about safe use of non-sterile alcohol prep pads
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Guidance - Target Animal Safety & Effectiveness Protocol Development & Submission
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Breaded Okra
  • From: FoodSafety.gov
• Magic Valley Fresh Frozen, Inc. Foods Issues Allergy Alert On Undeclared Milk In Breaded Okra
  • From: U.S. Food & Drug Administration (FDA)
• Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group's Alcohol Prep Products
  • From: U.S. Food & Drug Administration (FDA)
• Sabor Farms Recalls Four Brands Of Cilantro Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Fresh Cilantro
  • From: FoodSafety.gov
• FDA MedWatch - B. Braun Outlook 400ES Safety Infusion System, Model Number 621-400ES: Class I Recall - Hardware May Become Unresponsive
  • From: FDA MedWatch
• RECALL: Horse Feed Distributed in California, Nevada, and Oregon
  • From: FoodSafety.gov
• RECALL: Jr. Texas JR Taffy pet treat, possible Salmonella
  • From: FoodSafety.gov
• ALLERGY ALERTS: Ice Cream, Cheese, Veal Ravioli
  • From: FoodSafety.gov
• The February 2011 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - January 2011 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - two recalls - Family Farm Complete Horse 10 horse feed and Jr. Texas Taffy pet treat
  • From: U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Ice Cream Containing Undeclared Allergen
  • From: U.S. Food & Drug Administration (FDA)
• MERRICK PET CARE RECALLS JR TEXAS TAFFY PET TREAT (ITEM # 27077, ALL LOTS UP TO AND INCLUDING 10364) BECAUSE OF POSSIBLE SALMONELLA HEALTH RISK
  • From: U.S. Food & Drug Administration (FDA)
• Feed Manufacturer Issues Limited Voluntary Recall of a Horse Feed Product Distributed in California, Nevada, and Oregon
  • From: U.S. Food & Drug Administration (FDA)
• Undeclared Soy in "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread"
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Keebler Fudge Shoppe Jumbo Fudge Sticks sold at convenience stores
  • From: FoodSafety.gov
• RECALL: All Toxic Waste brand Nuclear Sludge Products
  • From: FoodSafety.gov
• KEEBLER ISSUES ALLERGY ALERT ON MISLABELED 8-COUNT CARTONS OF FUDGE SHOPPE® JUMBO FUDGE STICKS SOLD AT CONVENIENCE STORES
  • From: U.S. Food & Drug Administration (FDA)
• Candy Dynamics Expands Recall to all Toxic Waste® brand Nuclear Sludge® Products all flavors and all sizes
  • From: U.S. Food & Drug Administration (FDA)
• PEEKAY INTERNATIONAL INC. ISSUES ALLERGY ALERT ON UNDECLARED SULFITES IN SWAN GOLDEN RAISINS
  • From: U.S. Food & Drug Administration (FDA)
• Important information for ARIXTRA® Starter Kit patients regarding Triad Group's alcohol prep products
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Fourth FDA orphan drug designation workshop scheduled for Feb. 28 - March 1, 2011
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERTS: Calamari, Corn Pops, Shrimp, Potato Chips
  • From: FoodSafety.gov
• RECALL: Wide Variety of Salad Greens, Including Organic, Sold on the East Coast
  • From: FoodSafety.gov
• State Garden, Inc. Announces Voluntary Recall Of Certain Salad Mixes Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Pfizer Inc. And Progenics Alert Physicians And Patients To Information Related To Triad Group Alcohol Prep Products Included In U.S. RELISTOR Kit Packaging
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Breast Implants: FDA Review Indicates Possible Association With A Rare Cancer
  • From: FDA MedWatch
• FDA review indicates possible association between breast implants and a rare cancer
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Two of Ian's brand Frozen Entrees
  • From: FoodSafety.gov
• Ian's Voluntarily Recalls Two Products Due To Risk Of Contamination By Listeria Bacteria
  • From: U.S. Food & Drug Administration (FDA)
• King & Prince Seafood Issues Voluntary Recall Notice On Breaded Calamari Products
  • From: U.S. Food & Drug Administration (FDA)
• Kanec USA, Inc. Issues a Voluntary Recall of Nite Rider Maximum Sexual Enhancer For Men and STUD Capsules for Men Male Enhancement Herbal Supplement Capsules Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Mama Rose's Con Queso, Hopi Corn Salsa -- Possible Botulism Risk
  • From: FoodSafety.gov
• Pretzels. Inc. Issues Allergy Alert On Undeclared Milk In Better Made Brand Corn Pops
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Viibryd to treat major depressive disorder
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Availability of the NARMS Strategic Plan
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fresenius Medical Care CombiSet True Flow Series Hemodialysis Blood Tubing Set with Priming Set and Transducer Protectors: Class I Recall - Potential for Kinking of Arterial Line
  • From: FDA MedWatch
• Hawaii Business Group Incorporated, Barb's Favorite Recipes, and Ohana Seafoods Recall Barb's Local Style Black Bean Sauce and Ohana Flavors Black Bean Sauce Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Mama Rose's Gourmet Foods Recalls Cilantro Con Queso, Garlic Con Queso, Viper Venom Con Queso and Hopi Corn Salsa Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Important Information for Betaseron® (interferon beta 1-b) Consumers Regarding Triad Group's Alcohol Prep Products
  • 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)
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Maine seafood processor enters into consent decree with FDA
  • From: U.S. Food & Drug Administration (FDA)
• Rich Products Corporation announces nationwide voluntary recall of Sonny's Barbecue Deep Deveined Shrimp
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Barrel O' Fun Snack Foods Co. Issues Allergen Alert on Undeclared Milk Protein in
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 19, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA to improve most common review path for medical devices
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Toxic Waste® brand Nuclear Sludge® Chew Bars
  • From: FoodSafety.gov
• RECALL: Ossie's Schmaltz Herring
  • From: FoodSafety.gov
• RECALL: Winn-Dixie Beef Patties, OneGreat Hamburgers
  • From: FoodSafety.gov
• ALLERGY ALERT: Kroger Chocolate Chips Contain Milk
  • From: FoodSafety.gov
• FDA Approves Head Lice Treatment for Children and Adults
  • From: U.S. Food & Drug Administration (FDA)
• Commissioner's Fellowship Program
  • From: U.S. Food & Drug Administration (FDA)
• Federal government obtains permanent injunction against Deltex Pharmaceuticals Inc.
  • 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
  • From: U.S. Food & Drug Administration (FDA)
• Genentech Informs Customers Of Important Information About Triad Groups
  • From: U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products
  • From: U.S. Food & Drug Administration (FDA)
• MS Fish Corp Issues Alert On Listeria In
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Multaq (dronedarone)- Risk of Severe Liver Injury:Reports include two cases of liver failure leading to liver transplant
  • From: FDA MedWatch
• December 2010 Safety Labeling Changes: 58 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• Enforcement Report for January 12, 2011
  • From: U.S. Food & Drug Administration (FDA)
• FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings
  • From: U.S. Food & Drug Administration (FDA)
• Candy Dynamics Recalls Toxic Waste® brand Nuclear Sludge® Chew Bars
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA seeks to halt processing, distribution at New York juice company
  • From: U.S. Food & Drug Administration (FDA)
• Medicines in My Home Update
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - January 2011 Update on Feed Enforcement Activities to Limit the Spread of BSE
  • From: U.S. Food & Drug Administration (FDA)
• Barry Callebaut USA LLC Issues Allergen Alert on Potential Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize dental devices from Florida manufacturer
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetaminophen Prescription Products Limited to 325 mg Per Dosage Unit: Drug Safety Communication
  • From: FDA MedWatch
• FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Webinar Announcement - Question-Based Review - Part III: Sterile Process Validation
  • From: U.S. Food & Drug Administration (FDA)
• The January 2011 FDA Patient Safety News is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Surtex Foods Recalls "Oaxaca String Cheese La Original" Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Sprouters Northwest, Inc. Recalls Clover Sprouts and Clover Sprout Mixes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Ground Beef Distributed to Institutions in CA and OR
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL): Medication Use Error - Reports of Accidental Overdose
  • From: FDA MedWatch
• HIV/AIDS Update - Revised Adult HIV Treatment Guidelines available
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• AngioScore Incorporated Announces Worldwide Voluntary Field Removal of the AngioSculpt® PTA Scoring Balloon Catheter, 0.018" OTW, balloon sizes: 4.0x20mm, 5.0x20mm, and 6.0x20mm
  • From: U.S. Food & Drug Administration (FDA)
• La Placita Botanas Mexicanas, Inc. Recalls Wheat Snacks with Chile, Potato Chips with Chile, and Corn Churritos with Chile Because of Possible Contamination with Salmonella
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves opioid analgesic to help cancer patients manage pain
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of lamivudine and tenofovir DF 300 mg/300 mg fixed-dose combination
  • From: U.S. Food & Drug Administration (FDA)
• FDA warns public of continued extortion scam by FDA impersonators
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Working to Address Shortage of Injectable Iron Dextran - Status Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA inspects retailers in Miss.; issues warning letters for illegal tobacco sales to minors
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Cilantro & Parsley (Wegmans, Boncheff brands) in NY & PA
  • From: FoodSafety.gov
• ALLERGY ALERT: Beef, Turkey, and Chicken Tamales in CA, OR, WA
  • From: FoodSafety.gov
• Boncheff Greenhouses, Inc. Recalls For Wegmans Food Markets, Inc., Budwey Markets, Wades Market, Cuba Giant Food Market, And Hegedorn's Cilantro, Curly Parsley, And Italian Parsley Because Of A Possible Health Risk.
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of lamivudine and zidovudine tablets, 30 mg/60 mg fixed-dose combination
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Triad Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks: Recall Due to Potential Microbial Contamination
  • From: FDA MedWatch
• FDA MedWatch - Metronidazole Tablets, 250mg: Recall - Underweight Tablets
  • From: FDA MedWatch
• Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets
  • From: U.S. Food & Drug Administration (FDA)
• FDA launches website to help regulated industries save time, resources
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 5, 2011
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CVM is now accepting applications for its 2011 Student Summer Intern Program "Windows to Regulatory Research."
  • From: U.S. Food & Drug Administration (FDA)
• FDA to require substantial equivalence reviews for new tobacco products
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - AngioScore Inc., AngioSculpt Percutaneous Transluminal Angioplasty (PTA) Scoring Balloon Catheter OTW 0.018" Platform - Class I Recall
  • From: FDA MedWatch
• RECALL: Sprouts in WA, OR, ID and AK
  • From: FoodSafety.gov
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Basics Webinar: State Enforcement Program
  • From: U.S. Food & Drug Administration (FDA)
• The January 2011 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• SPROUTERS NORTHWEST, INC. RECALLS CLOVER SPROUTS AND CLOVER SPROUT MIXES BECAUSE OF POSSIBLE HEALTH RISK
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts
  • From: U.S. Food & Drug Administration (FDA)
• PRock Marketing, LLC Issues a Voluntary Nationwide Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement.
  • From: U.S. Food & Drug Administration (FDA)
• The Ritedose Corporation Announces the Voluntary Nationwide Recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL Due to Mislabeled Unit Dose Vials
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Albuterol Sulfate Inhalation Solution 0.083%, 3 mL Unit Dose Vials: Recall - Mislabeled Unit Dose Vials
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Minor Use and Minor Species (MUMS) Grant Program Request for Applications
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Breaded Chicken Wing Products with Egg Distributed to Restaurants
  • From: FoodSafety.gov
• RECALL: Organic Ground Beef Sold in CA, NJ, NY, NC, WI, WA
  • From: FoodSafety.gov
• FDA warns consumers not to use Fruta Planta weight loss products
  • From: U.S. Food & Drug Administration (FDA)
• Drive Total Energy Issues a Voluntary Recall of Rock Hard Extreme and Passion Coffee Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetadote (acetylcysteine) Injection: Recall - Particulate Matter Found in a Small Number of Vials
  • From: FDA MedWatch
• ALLERGY ALERT: Cuernos (Croissants)
  • From: FoodSafety.gov
• ALLERGY ALERT: Teriyaki Beef Jerky with Wheat
  • From: FoodSafety.gov
• Recall: Fresh Greens, Herbs, Other Produce
  • From: FoodSafety.gov
• Recall: Alfalfa Sprouts
  • From: FoodSafety.gov
• Mexicantown Wholesale Issues Allergy Alert For Undeclared Milk in Cuernos (Croissants)
  • From: U.S. Food & Drug Administration (FDA)
• TINY GREENS ORGANIC FARM FOOD CO. RECALLS PRODUCT BECAUSE OF POSSIBLE HEALTH RISK
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 29, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arrow Intra-Aortic Balloon (IAB) Catheter Products: Class 1 Recall - Catheters can become Stuck in the Sheath
  • From: FDA MedWatch
• J&D Produce Announces Precautionary, Voluntary Recall Of Fresh Greens
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Bicarbonate Injection, USP, 7.5% and 8.4%, 50 mL Single Dose Vials - Recall Due to Particulates in Some Vials
  • From: FDA MedWatch
• ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• ev3 NanoCross .014" OTW PTA Dilatation Catheter: Class I Recall - Potential for cracking or breaking
  • From: FDA MedWatch
• FDA: Don't Eat Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts
  • From: U.S. Food & Drug Administration (FDA)
• Brand Castle, LLC Issues Allergy Alert On Undeclared Egg In Icing Of Licensed Rice Krispies Treats Holiday Village Kit Distributed Through Michaels Retail Stores Only
  • From: U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces A Recall Of Products Which Were Produced By Rolf's Patisserie In Seven States In The Midwest Because Of A Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces A Recall For Ginger Bread Houses Which Were Produced By Rolf's Patisserie In Twenty-Three States Because Of A Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Abbott Diabetes Care Announces Recall of Certain Lots of Precision Xtra®, Precision Xceed Pro®, MediSense® Optium[TM], Optium[TM], OptiumEZ and ReliOn® Ultima Blood Glucose Test Strips in the United States and Puerto Rico
  • From: U.S. Food & Drug Administration (FDA)
• JFC International Inc. Recalls "Frozen Capelin" Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• South Florida Bakery Issues Recall for Publix Bakery Coconut Macaroons (Coquitos)
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Rolf's Patisserie recalling all desserts made after November 1
  • From: U.S. Food & Drug Administration (FDA)
• Dexamethasone Sodium Phosphate Injection, 4 mg/mL, 30 mL Multiple Dose Vial: Recall due to Particulates in Product
  • From: FDA MedWatch
• FDA MedWatch - Fruta Planta: Public Notification - Undeclared Drug Ingredient
  • From: FDA MedWatch
• FDA MedWatch - RockHard Weekend, Pandora: Recall - Undeclared Drug Ingredient
  • From: FDA MedWatch
• HIV/AIDS Update - New Intelence (etravirine) dosage approved
  • From: U.S. Food & Drug Administration (FDA)
• Pfizer To Recall One Lot Of Lipitor In The U.S.
  • From: U.S. Food & Drug Administration (FDA)
• RockHard Laboratories Issues a Voluntary Recall of Specific Lots of the Dietary Supplements RockHard Weekend and Pandora
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Gardasil approved to prevent anal cancer
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Recombinant Human Growth Hormone (somatropin): Ongoing Safety Review - Possible Increased Risk of Death
  • From: FDA MedWatch
• Shining a Light on Insurance Companies
  • From: HealthCare.gov
• FDA announces recall of Abbott glucose test strips
  • From: U.S. Food & Drug Administration (FDA)
• RECALLS: Frozen capelin fish and
  • From: FoodSafety.gov
• FDA MedWatch - Abbott Glucose Test Strips: Recall - False Low Blood Glucose Results
  • From: FDA MedWatch
• IMPF Voluntarily Recalls Dips & Spreads because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 22, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Secretary of Health and Human Services Announces 2011 Healthy Living Innovation Awards
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces Cheese Recall For Products In Three Western States And Washington, D.C. Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• JFC International Inc Issues An Alert On Uneviscerated Fish
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fresenius Kabi LLC, Red Blood Cell (RBC) Exchange Sets used on AS104 Blood Cell Separation Devices: Class I Recall
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• HHS and Walgreens Announce New Effort Aimed at Addressing Health Disparities in Flu Vaccination
  • From: U.S. Dept. of Health & Human Services
• Kroger Recalls Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• YNOT FOODS INC. Issues Allergy Alert on Undeclared Milk and Soybean in Upsides[TM] Orzo Toscano, 6/2.5lb
  • From: U.S. Food & Drug Administration (FDA)
• Tofutti Brands Inc. Announces Updated Information for Recall of 25 Pallets of Yours Truly Frozen Dessert Cones Due to Possible Trace Level Milk Contamination
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) BadAd Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kroger Recalls Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - NARMS Retail Meat Annual Report, 2008
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Consumers should not eat Sally Jackson cheese due to risk of Escherichia coli O157:H7
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: All Sally Jackson Cheese
  • From: FoodSafety.gov
• FDA MedWatch - Anzemet (dolasetron mesylate): Drug Safety Communication - Reports of Abnormal Heart Rhythms
  • From: FDA MedWatch
• Sally Jackson Cheese Recalls All Cheese Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avastin (bevacizumab): Process for Removal of Breast Cancer Indication Begun
  • From: FDA MedWatch
• FDA Hepatitis Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination
  • From: U.S. Food & Drug Administration (FDA)
• FDA begins process to remove breast cancer indication from Avastin label
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Issue of FDA Veterinarian Newsletter!
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 15, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA: Tainted products marketed as dietary supplements potentially dangerous
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Brinkman's Gourmet Barbecue Sauce
  • From: FoodSafety.gov
• Update of CVM's What's New - December 2010 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• Brinkman Turkey Farms Inc. Issues Allergy Alert On Undeclared Soy And Milk In "Brinkman's Gourmet Barbecue Sauce".
  • From: U.S. Food & Drug Administration (FDA)
• FDA says Tessalon liquid cough capsules pose risk for young children
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tessalon (benzonatate): Drug Safety Communication - Potential for Accidental Ingestion by Children
  • From: FDA MedWatch
• FDA MedWatch - Rolaids Extra Strength Softchews, Rolaids Extra Strength plus Gas Softchews, Rolaids Multi-Symptom plus Anti-Gas Softchews: Recall - Foreign Materials in Products
  • From: FDA MedWatch
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Walnuts with Salmonella
  • From: FoodSafety.gov
• H1N1 Vaccine Safe and Induces Robust Immune Response in People with Asthma
  • From: U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) New FDA Basics Summary Metrics
  • From: U.S. Food & Drug Administration (FDA)
• Tropical Nut & Fruit of Charlotte, NC Announces a Nationwide Voluntary Recall of Walnut Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Announces Voluntary Recall Of All Lots Of Rolaids® Extra Strength Softchews, Roldaids® Extra Strength Plus Gas Softchews, And Roldaids® Multi-Symptom Plus Anti-Gas Softchews Sold In The United States
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in New Mexico
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Updated: With Table - Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled.
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New labeling approved for Prezista (darunavir)
  • From: U.S. Food & Drug Administration (FDA)
• Toffutti Brands Inc. Announces Recall Of 25 Pallets Of Yours Truly Frozen Dessert Cones Due To Possible Trace Level Milk Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Man Up Now Capsules: Consumer Warning - Undeclared Drug Ingredient
  • From: FDA MedWatch
• ALLERGY ALERT: Sauteed Chicken Products Sold to Restaurants in CA and HI
  • From: FoodSafety.gov
• FDA MedWatch - Reese Pharmaceutical Company OTC Products: Recall - Mislabeled Guaifenesin Tablets
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled.
  • From: U.S. Food & Drug Administration (FDA)
• FDA warns consumers to avoid Man Up Now capsules
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -New labeling for Zerit capsules and Zerit for oral solution
  • From: U.S. Food & Drug Administration (FDA)
• Mojave Foods Corporation Initiates Recall Due to Possible Health Risk from Walnut Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Reports on Antimicrobials Sold or Distributed for Food-Producing Animals
  • From: U.S. Food & Drug Administration (FDA)
• RECALLS: Cilantro, Pork Products, Dried Fish
  • From: FoodSafety.gov
• FDA issues guidance on public comment procedures at advisory committee meetings
  • From: U.S. Food & Drug Administration (FDA)
• Pablo's Produce, Inc. Recalls One Lot of Cilantro because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 8, 2010
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Penumbra System Reperfusion Catheter 032: Class I Recall Due to Manufacturing Error
  • From: FDA MedWatch
• November 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions
  • From: FDA MedWatch
• A Flu Vaccine that Lasts: NIH Scientists Consider Prospects for a Universal Influenza Vaccine
  • From: U.S. Dept. of Health & Human Services
• Presidential Proclamation--National Influenza Vaccination Week
  • From: U.S. Dept. of Health & Human Services
• S&S Food Inc. Issues An Alert On Uneviscerated Fish
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• The December 2010 FDA Patient Safety News is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Wisconsin Business Recalls Smoked Fish Spread; May Be Contaminated With Listeria
  • From: U.S. Food & Drug Administration (FDA)
• National Influenza Vaccination Week to be held December 5-11, 2010
  • From: U.S. Dept. of Health & Human Services
• Seasonal Flu and 2009 H1N1 Flu Vaccination Coverage Among Pregnant Women, 2009--10 Flu Season
  • From: U.S. Dept. of Health & Human Services
• Lobby Shoppes, Inc. Issues An Allergy Alert On Milk And Soy Products In "Cheese Popcorn, Chicago Triple Mix Popcorn And Caramel Corn"
  • From: U.S. Food & Drug Administration (FDA)
• California Firm Recalls Chicken Tamales Due To Mislabeling and an Undeclared Allergen
  • From: FoodSafety.gov
• RECALL: Bumble Bee Chicken Salad
  • From: FoodSafety.gov
• Intelli Health Products, Issues an Expansion to All Lots of their Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA seeking new members with Hep C experience for its Antiviral Drugs Advisory Committee
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves First Drug to Prevent Life Threatening Disease in Horses
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: NY Gourmet Salads
  • From: FoodSafety.gov
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Guidance - Residual Solvents in Animal Drug Products
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of rapid INSTI[TM] HIV-1 Antibody Test
  • From: U.S. Food & Drug Administration (FDA)
• Recall of Mylanta and Alternagel Liquid Products
  • From: U.S. Food & Drug Administration (FDA)
• Special Edition OWH eUpdate
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - November 2010 Green Book Update
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Frontier and Whole Foods Nutmeg
  • From: FoodSafety.gov
• Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Nutmeg
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 1, 2010
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• B. Braun addEASE Binary Connector: Class I Recall -Stopper Fragments May Enter Bag
  • From: FDA MedWatch
• ALLERGY ALERT: Golden Dipt® Fry Easy All-Purpose Batter
  • From: FoodSafety.gov
• The December 2010 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• McCormick & Company Recalls Golden Dipt® Fry Easy All-Purpose Batter Due To Unlabeled Egg Ingredient
  • From: U.S. Food & Drug Administration (FDA)