FDA News Releases

• Date Index

• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, (continued)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals November 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• House of Spices (India) Inc. ISSUES ALERT ON UNDECLARED SULFITES IN “GOLDEN RAISIN”, U.S. Food & Drug Administration (FDA)
• House of Spices (India) Inc. Issues Alert on Undeclared Sulfites in "Golden Raisin", U.S. Food & Drug Administration (FDA)
• Oasis Brands, Inc. Retira Productos Lacteos Santa Martha debido a Posible de Riesgos a la Salud, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 05, 2014, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update: Changes to Olysio (simeprevir) label, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hospira, GemStar Power Supply, 3VDC, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GemStar Power Supply, 3VDC for GemStar Infusion Pumps by Hospira: Class I Recall - Power Supply May Not Deliver Enough Electricity, FDA MedWatch
• Welcome Market, Inc. dba 99 Ranch Market Announces Recall of “Taro Toast”, “Family Toast”, “U-Ta-Ne Toast”, “Raisin Toast”, “Green Onion Porksung Toast”, “Coconut Toast”, “Pineapple Toast”, “Multi-9 Grain”, “Cheese Toast”, “Wheat Bran Toast”, and “Red Bean Toast”, U.S. Food & Drug Administration (FDA)
• New Jersey Firm Issues Allergy Alert on Undeclared Fish, Wheat and Egg In Garden Rotini Salad, U.S. Food & Drug Administration (FDA)
• Kids.gov para celebrar el Día Nacional del Niño, GobiernoUSA.gov
• Update of CVM's What's New - FDA Ensures Your Foods From Animals Are Safe, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bartlett Milling Company Issues Recall of Horse Food, U.S. Food & Drug Administration (FDA)
• Bartlett Milling Company Issues Recall of Horse Food, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - November 2014, U.S. Food & Drug Administration (FDA)
• Marathon Ventures, Inc. Announces Voluntary Recall of Raw Macadamia Nuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 10 Percent Neutral Buffered Formalin by Richard-Allan Scientific: Class I Recall - May Contain Incorrect Concentration of Formalin, FDA MedWatch
• Medical Device Safety and Recalls: Richard-Allan Scientific, 10% Neutral Buffered Formalin, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 29, 2014, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • <Possible follow-ups>
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
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  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
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  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
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  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
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  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
• Update of CVM's What's New - FDA Basics Webinar November 5, 2014: CVM’s Pet Food Reporting and Recall Process, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Presentations, Q&A, and Transcript now available for the Data Quality Webinar, U.S. Food & Drug Administration (FDA)
• Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
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  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
• First vaccine approved by FDA to prevent serogroup B Meningococcal disease, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Shur-Green Farms Issues Voluntary Nationwide Recall of Lascadoil/Soyoil Due to Possible Lasalocid Contamination, U.S. Food & Drug Administration (FDA)
• Chetak New York L.L.C. Recalls 7 Oz., 14 Oz., & 28 Oz. Packages of "Deep Raw Cashew Pieces" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Melrose Recalls Vegan Gingersnap Cookies Due to Mislabeling and Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Shur-Green Farms Issues Voluntary Nationwide Recall of Lascadoil/Soyoil Due to Possible Lasalocid Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baby Wipes by Nutek Disposables, Inc.: Recall - May Contain Bacteria, FDA MedWatch
• Z Natural Foods Recalls Lightly Roasted Organic Carob Powder Due to Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Rome Packing Co., Inc. Recalls Fresh And Frozen Crab Meat Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lundberg Family Farms Recalls Sea Salt Rice Chips Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Baxter Initiates Voluntary Recall of Two Lots of Intravia Containers in the U.S. and Canada, U.S. Food & Drug Administration (FDA)
• Nutek Disposables, Inc. Issues Alert Due to Potential Bacteria in Baby Wipes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Intravia Containers by Baxter: Recall - Particulate Matter, FDA MedWatch
• FDA approves new treatment for rare form of hemophilia, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 22, 2014, U.S. Food & Drug Administration (FDA)
• Bailey Farms Inc. Recalls Fresh Serrano Chile Peppers Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA Public Meeting: Supplemental Notices of Proposed Rulemaking, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Assured Brand Naproxen Sodium Tablets by Contract Packaging Resources, Inc.: Recall - Packaging Mix-Up, FDA MedWatch
• Contract Packaging Resources, Inc. Issues a Voluntary Nationwide Recall of Assured Brand Naproxen Sodium Tablets due to Packaging Mix-Up, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Covidien, Medi-Trace Cadence and Kendall Defibrillation Electrodes, U.S. Food & Drug Administration (FDA)
• AMS Health Sciences, LLC Issues Voluntary Recall of Saba Shark Cartilage Complex, 60 Capsule Bottles Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Oasis Brands, Inc. Recalls Products Lacteos Santa Martha Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall of Publix Asian Mix, U.S. Food & Drug Administration (FDA)
• United Natural Trading LLC dba/ Woodstock Farms Manufacturing Issues Allergy Alert for Undeclared Peanuts in Asian 7 Rice Cracker Mix, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCI Injection, USP 10 MG Per ML, 30 ML Single-Dose. Preservative-Free, Due To Particulate Matter, U.S. Food & Drug Administration (FDA)
• Lidocaine HCI Injection, USP 10 MG Per ML, 30 ML Single-Dose. Preservative-Free, by Hospira: Recall - Particulate Matter, FDA MedWatch
• Cómo enviar un paquete a nuestras tropas en el extranjero, GobiernoUSA.gov
• FDA approves labeling with abuse-deterrent features for third extended-release opioid analgesic, U.S. Food & Drug Administration (FDA)
• New Hope Mills Issues Allergy Alert on Undeclared Soy in New Hope Mills Gluten Free Chia Pancake and Waffle Mix, U.S. Food & Drug Administration (FDA)
• FDA Supports National Mammography Day, FDA Office of Women's Health
• CVM Updates - FDA Issues Draft Guidance with Recommendations for Drug Sponsors Submitting Two-Phased Chemistry, Manufacturing, and Controls Technical Data, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 15, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - September 2014 Safety Labeling Changes posting includes 55 products with changes to Prescribing Information, FDA MedWatch
• FDA approves Ofev to treat idiopathic pulmonary fibrosis, U.S. Food & Drug Administration (FDA)
• FDA approves Esbriet to treat idiopathic pulmonary fibrosis, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - LifeCare Flexible Intravenous Solutions by Hospira, Inc.: Recall - Potential for Leakage, FDA MedWatch
• Covidien Initiates Voluntary Field Safety Alert for Medi-Trace™ Cadence and Kendall™ Multi-function Defibrillation Electrodes, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall Of Certain Lots of Several Lifecare Products Due To Potential For Leakage, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • <Possible follow-ups>
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
  • FoodSafety.gov Recalls & Alerts Update, FoodSafety.gov
• FDA permits marketing of urinary prosthesis device for women, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA permits marketing of urinary prosthesis device for women, FDA Office of Women's Health
• Real Foods Of Seattle, LLC Issues Allergy Alert On Undeclared Egg In Mexican Cheddar Dip, FoodSafety.gov
  • <Possible follow-ups>
  • Real Foods Of Seattle, LLC Issues Allergy Alert On Undeclared Egg In Mexican Cheddar Dip, U.S. Food & Drug Administration (FDA)
• Sunburst Foods Recalls Products Because Of Possible Health Risk, FoodSafety.gov
  • <Possible follow-ups>
  • Sunburst Foods Recalls Products Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• California Olive And Vine Announces The Voluntary Recall Of Pumpkin Seed Pesto, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • California Olive And Vine Announces The Voluntary Recall Of Pumpkin Seed Pesto, FoodSafety.gov
• California Firm Expands Recall of Beef Products Due To Possible Processing Flaw, FoodSafety.gov
• Medi-Trace Cadence and Kendall Multi-function Defibrillation Electrodes by Covidien: Field Safety Alert - Electrodes Will Not Connect with Philips FR3 or FRx AED unit, FDA MedWatch
• FDA approves first combination pill to treat hepatitis C, U.S. Food & Drug Administration (FDA)
• FDA approves a new ultrasound imaging agent, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval of Harvoni fixed-dose combination tablet (ledipasvir and sofosbuvir) for treatment of Hepatitis C, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Hepatitis Update - Approval of Harvoni fixed-dose combination tablet (ledipasvir and sofosbuvir) for treatment of Hepatitis C, U.S. Food & Drug Administration (FDA)
• FDA approves first drug-coated angioplasty balloon catheter to treat vascular disease, U.S. Food & Drug Administration (FDA)
• FDA approves Akynzeo for nausea and vomiting associated with cancer chemotherapy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Oregon Compounding Centers, Inc. Unexpired Sterile Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• FDA MedWatch - ICU Medical ConMed Stat2 Flow Controller: Class 1 Recall - Delivers Higher Flow Rate than Intended, FDA MedWatch
• FDA MedWatch - CareFusion EnVe and ReVel Ventilators: Class 1 Recall - Power Connection Failure, FDA MedWatch
• Update of CVM's What's New - Oregon Compounding Centers, Inc. Issues Voluntary Recall of Unexpired Sterile Products in Oregon and Washington Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Oregon Compounding Centers, Inc. Issues Voluntary Recall of Unexpired Sterile Products in Oregon and Washington Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Allergy Alert On Undelcared Eggs In Lotte Waffles, FoodSafety.gov
• Update of CVM's What's New - Updated Public Master Files (PMFs) Supporting Applications for Minor Use and Minor Species Drugs in Development, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: CareFusion 203, Inc., EnVe and ReVel ventilators - Power Connection Failure, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: ICU Medical, Inc., ConMed Stat2 Flow Controller – Delivers Higher Flow Rate than Intended, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 07, 2014, U.S. Food & Drug Administration (FDA)
• Oasis Brands, Inc Recalls Cuajada en Hoja 12oz because of Possible Health Risk, FoodSafety.gov
  • <Possible follow-ups>
  • Oasis Brands, Inc Recalls Cuajada en Hoja 12oz because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vancomycin Hydrochloride for Injection USP, Equivalent to 1 Gram Vancomycin (Sterile Powder) by Hospira, Inc.: Recall - Uncontrolled Storage During Transit, FDA MedWatch
• FDA MedWatch - SAM Junctional Tourniquet Accessory (Axilla) Strap/SAM Medical Products: Recall - Potential Clip Failure, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Vancomycin Hydrochloride for Injection USP, Equivalent to 1 G Vancomycin (Sterile Powder) Due to Uncontrolled Storage During Transit, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Final Guidance on Terminology for Veterinary Medicinal Products Adverse Event Reporting, U.S. Food & Drug Administration (FDA)
• SAM Medical Products Implements Voluntary Recall of its Accessory (Axilla) Strap for the SAM Junctional Tourniquet, U.S. Food & Drug Administration (FDA)
• Minnesota Firm Recalls Meat and Poultry Products for Possible Listeria Contamination, FoodSafety.gov
• J&b European Distribution Inc. Issues Allergy Alert For Undeclared Milk In Kupiec Rice Cakes With Dark Chocolate, FoodSafety.gov
  • <Possible follow-ups>
  • J&b European Distribution Inc. Issues Allergy Alert For Undeclared Milk In Kupiec Rice Cakes With Dark Chocolate, U.S. Food & Drug Administration (FDA)
• HAR Maspeth Corp RECALLS Jinga brand “Pan Fried Anchovies� BECAUSE OF POSSIBLE HEALTH RISK, FoodSafety.gov
  • <Possible follow-ups>
  • HAR Maspeth Corp RECALLS Jinga brand “Pan Fried Anchovies� BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hudson RCI Pediatric Anesthesia Breathing Circuits by Teleflex Medical: Class I Recall - Circuit Ends May Crack or Break, FDA MedWatch
• Update of CVM's What's New - Inspections, Recalls, and Other Actions with Respect to Firms that Engage in Animal Drug Compounding, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Teleflex Medical, Hudson RCI Pediatric Anesthesia Breathing Circuits, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ketorolac Tromethamine Injection, USP, 30mg/ml by Sagent Pharmaceuticals: Recall - Incorrect Labeling, FDA MedWatch
• Markpol Distributors Inc. Issues Allergy Alert on Undeclared Milk in Kupiec Rice Cakes with Dark Chocolate, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Ketorolac Tromethamine Injection, USP, 30mg/Ml Due to Labeling the Product With the Incorrect Expiration Date, U.S. Food & Drug Administration (FDA)
• FDA seeks permanent injunction against Pharmaceutical Innovations, Inc., U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 01, 2014, U.S. Food & Drug Administration (FDA)
• The October 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Alivio tributario para sobrevivientes de ataques terroristas, GobiernoUSA.gov
• Update of CVM's What's New - Animal Drug Approvals October 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• CVM Updates - NARMS 2011 Executive Report - Interactive Data Displays, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Annual Summary Report on Antimicrobials Sold or Distributed in 2012 for Use in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• IKEA Recalls PASTAÄLGAR FULLKORN And PASTAÄLGAR, Due To Non-Declared Soy Content, U.S. Food & Drug Administration (FDA)
• Tropical Valley Foods Issues Allergy Alert For Potentially Undeclared Peanuts In Next By Nature Dark Chocolate Cherries, U.S. Food & Drug Administration (FDA)
• 3D Technologies: A New Era in Breast Cancer Detection, FDA Office of Women's Health
• The FDA takes steps to strengthen cybersecurity of medical devices, U.S. Food & Drug Administration (FDA)
• FDA awards grants to stimulate drug, device development for rare diseases, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Publishes Target Animal Safety Data to Support Drug Applications for Potassium Bromide to Control Seizures in Dogs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo Recalls Select Chicken and Turkey Pet Foods Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Bravo Recalls Select Chicken and Turkey Pet Foods Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Dominguez Foods of Washington Inc. Issues Allergy Alert on Undeclared Wheat, Whey (Milk), and Soy in “Su Cocina” Label, Pan Molido (Plain Bread Crumbs), U.S. Food & Drug Administration (FDA)
• Whole Foods Market Bedford Recalls Streusel Coffee Cake Due To Undeclared Tree Nut Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bo Ying Compound by Eu Yan Sang (Hong Kong) Ltd: FDA/CDER Statement - Risk of Lead Poisoning, FDA MedWatch
• FDA MedWatch - Xolair (omalizumab): Drug Safety Communication - Slightly Elevated Risk of Cardiovascular and Cerebrovascular Serious Adverse Events, FDA MedWatch
• CVM Updates - Food Facility Biennial Registration Renewal, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 24, 2014, U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health e-Update: September - October 2014, FDA Office of Women's Health
• HIV/AIDS Update - Approval of Vitekta, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of Tybost (cobicistat) 150 mg tablets, U.S. Food & Drug Administration (FDA)
• The Original Soupman Issues Allergy Alert and Recall on Certain Lots of “The Original Soupman Lobster Bisque”, U.S. Food & Drug Administration (FDA)
• Gold Star Smoked Fish Corp. Voluntarily Recalls Cold Smoke Steelhead Due to Possible Listeria Monocytogenes Contamination., U.S. Food & Drug Administration (FDA)
• Si quiere abrir su propio negocio esta charla es para usted, GobiernoUSA.gov
• FDA food safety challenge to spur new technologies for fighting foodborne illness, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance Recommending Global Standards for Bioequivalence Study, U.S. Food & Drug Administration (FDA)
• Consumer Alert: Undeclared Eggs in “Coconut Bun”, U.S. Food & Drug Administration (FDA)
• Glaser Organic Farms Recalls Organic Carob Powder For Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of the first test to identify five yeast pathogens directly from a blood sample, U.S. Food & Drug Administration (FDA)
• Mars Chocolate North America Issues Allergy Alert Voluntary Recall On Undeclared Peanut Butter In M&Ms Brand Milk Chocolate Theater Box, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Seeks to Make FSMA Proposals More Flexible, Targeted, U.S. Food & Drug Administration (FDA)
• Celebre el Mes de la Herencia Hispana, GobiernoUSA.gov
• Enforcement Report for September 17, 2014, U.S. Food & Drug Administration (FDA)
• An Alert on Uneviscerated Dried Roach (Vobla), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Combating Antibiotic Resistance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Research Helps Keep Animals—and People—Healthy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Potassium Chloride Injection (Baxter): Recall - Shipping Carton Mislabeling, FDA MedWatch
• Cómo evitar la violencia juvenil en sus hijos, GobiernoUSA.gov
• Baxter Initiates U.S. Voluntary Recall of One Lot of Potassium Chloride Injection Due to Shipping Carton Mislabeling, U.S. Food & Drug Administration (FDA)
• Gel Spice Company, Inc. Issues A Voluntary Recall Of Fresh Finds Brand Ground Black Pepper, 3.53 oz (100 g), Due To Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Mantenga la seguridad vehicular de sus niños usando el asiento correcto, GobiernoUSA.gov
• Playtex Adds Production Lot To Its March 2014 Voluntary Recall Of Certain AC/DC Power Adapters Used With the Playtex&reg; Nurser Deluxe Double Electric Breast Pump, U.S. Food & Drug Administration (FDA)
• Taylor Farms Pacific, Inc. voluntarily recalls Roma Tomatoes due to potential Salmonella contamination, U.S. Food & Drug Administration (FDA)
• La nueva Guía del Consumidor ya está disponible, GobiernoUSA.gov
• FDA MedWatch - August 2014 Safety Labeling Changes posting includes 32 products with changes to Prescribing Information, FDA MedWatch
• HIV/AIDS Update - Tentative approval of emtricitabine and tenofovir disoproxil fumarate fixed dose combination tablets, 200 mg/300 mg co-packaged with nevirapine tablets, 200 mg, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), In 0.9 percent Sodium Chloride Injection, 500 mL by Hospira: Recall - Particulate Matter, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), In 0.9 percent Sodium Chloride Injection, 500 Ml, Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - OLYSIO (simeprevir) label revisions, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Conditional Approval Explained: A Resource for Veterinarians, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 10, 2014, U.S. Food & Drug Administration (FDA)
• FDA reminds health care professionals and consumers not to use sterile products from Downing Labs/NuVision Pharmacy of Texas, U.S. Food & Drug Administration (FDA)
• Publix Recalls Private Label Jalapeno Bagels, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals September 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Plum Organics Voluntarily Recalls Little Cremes Organic Rice Milk Snacks Due to Potential Choking Hazard, U.S. Food & Drug Administration (FDA)
• Tullia's Recalls Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Mars Chocolate North America Issues Allergy Alert Voluntary Recall on Undeclared Peanuts and Eggs in TWIX® Bites 7oz Stand Up Pouch, U.S. Food & Drug Administration (FDA)
• Pharmacy Creations Issues Voluntary Recall of Four Product Lots With Limited Distribution in Florida, New Jersey, New York, and Puerto Rico Due to Potential Non-Sterility, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pharmacy Creations Certain Products: Recall – Potential Non-Sterility, FDA MedWatch
• Medical Device Safety and Recalls: Customed Inc., Surgical Convenience Packs - Damaged Packaging, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval: Lamivudine and Zidovudine Fixed Dose Combination Tablets, 150 mg/300 mg Co-packaged with Efavirenz Tablets, 600 mg, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of the first test to assess risk of developing acute kidney injury, U.S. Food & Drug Administration (FDA)
• Google reembolsará miles de dólares a usuarios de Android, GobiernoUSA.gov
• Medical Device Safety and Recalls: Cook CloverSnare 4-Loop Vascular Retrieval Snare - Snare Tip May Break During Use, U.S. Food & Drug Administration (FDA)
• Tullia’s Recalls Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 03, 2014, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize drug products from Flawless Beauty, U.S. Food & Drug Administration (FDA)
• The September 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves Keytruda for advanced melanoma, U.S. Food & Drug Administration (FDA)
• Encuentre ayuda gratis para dejar de fumar y beber alcohol, GobiernoUSA.gov
• La Orocovena Biscuit Voluntarily Recalls Pound Cake de Queso Due to Undeclared Milk, Soy and Wheat, U.S. Food & Drug Administration (FDA)
• Tjs Place recalls Basil Pesto Pasta because of potential health risk, U.S. Food & Drug Administration (FDA)
• We want to keep you updated!, The HealthCare.gov Team
• FDA MedWatch - Martin Avenue Pharmacy, Inc. Compounded Sterile Preparations: Recall - Lack of Assurance of Sterility, FDA MedWatch
• Martin Avenue Pharmacy, Inc. Issues a Voluntary Multi-State Recall of All Compounded Sterile Preparations Due to a Lack of Assurance of Sterility, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Dermatend Original and Dermatend Ultra: Recall - Safety Concerns, FDA MedWatch
• Update of CVM's What's New - My Dog Has Cancer: What Do I Need to Know?, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - PEDIGREE® Adult Complete Nutrition Limited Recall Due to Metal Fragments, U.S. Food & Drug Administration (FDA)
• PEDIGREE Adult Complete Nutrition Limited Recall Due to Metal Fragments (Expanded), U.S. Food & Drug Administration (FDA)
• Solace International, Inc. Issues Voluntary Nationwide Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns, U.S. Food & Drug Administration (FDA)
• Regeneca Worldwide, a Division of Vivaceuticals, Inc Expands the Voluntarily Recall of Regeneslim Appetite Control Capsules Due to the Presence of DMAA that May Pose Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kraft Foods Group Voluntarily Recalls Select Varieties of Regular Kraft American Singles Pasteurized Prepared Cheese Product Due to Ingredient Supplier's Out-of-Standard Storage Temperatures, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Stribild labeling update, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance Recommending Global Standard Format for Veterinary Medical Products Electronic Records, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Warning Letters for Unapproved Tear Stain Removers Used in Dogs and Cats, U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Announces Allergy Alert and Voluntary Limited Recall of DOLE-branded Spinach Due to Possible Contamination by Walnuts, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 27, 2014, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Takes Steps to Strengthen Program to Assess the Safety of Chemicals in Foods, Other Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - DePuy Synthes Craniomaxillofacial Distraction System: Class I Recall - May Reverse Directions After Surgery, FDA MedWatch
• Update of CVM's What's New - Mars Petcare US Announces Voluntary Recall of 22 Bags of PEDIGREE® Brand Adult Complete Nutrition for Dogs, U.S. Food & Drug Administration (FDA)
• Mars Petcare US Announces Voluntary Recall of 22 Bags of PEDIGREE® Brand Adult Complete Nutrition for Dogs Sold at Dollar General in Mississippi, Arkansas, Tennessee and Louisiana, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: DePuy Synthes Craniomaxillofacial Distraction System - May Reverse Directions After Surgery, U.S. Food & Drug Administration (FDA)
• UPDATED: CloverSnare? 4-Loop Vascular Retrieval Snare Recall, U.S. Food & Drug Administration (FDA)
• Voluntary Recall Notice of Margaret Holmes 14.5 oz Turnip Greens and 14.5 oz Mixed Greens Due to Questionable Seals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Convenience Surgical Packs by Customed, Inc.: Recall - Potential Loss of Sterility, FDA MedWatch
• Customed, Inc. Issues Recall of Sterile Convenience Surgical Packs, U.S. Food & Drug Administration (FDA)
• Approval of new fixed dose combination, TRIUMEQ (abacavir sulfate, dolutegravir, lamivudine), U.S. Food & Drug Administration (FDA)
• Nestlé Prepared Foods Company Announces Allergy Alert and Voluntary Recall Of LEAN CUISINE® Culinary Collection Chicken with Peanut Sauce Recall Due to Package Mislabeling, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Children’s Medical Ventures Gel-E Donut and Squishon 2: Class 1 Recall - Possibility of Mold, FDA MedWatch
• Labeling update for Intelence (etravirine), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Children’s Medical Ventures, Gel-E Donut and Squishon 2 - Possibility of Mold, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 20, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CloverSnare 4-Loop Vascular Retrieval Snare by Cook Medical: Recall - Risk of Loop to Separate From Shaft, FDA MedWatch
• CloverSnare&trade; 4-Loop Vascular Retrieval Snare Recall, U.S. Food & Drug Administration (FDA)
• nSPIRED Natural Foods, Inc. Voluntarily Recalls Certain Retail Lots Of Arrowhead Mills® Peanut Butters, Maranatha® Almond Butters And Peanut Butters And Specific Private Label Nut Butters Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Diamondback 360 Peripheral Orbital Atherectomy System by Cardiovascular Systems: Class I Recall - Sheath May Fracture During Use, FDA MedWatch
• Medical Device Safety and Recalls: Cardiovascular Systems Diamondback 360 Peripheral Orbital Atherectomy System, U.S. Food & Drug Administration (FDA)
• Conozca los programas escolares de nutrición infantil, GobiernoUSA.gov
• FDA MedWatch - Dianeal Low Calcium (2.5mEq/L) Peritoneal Dialysis Solution with 2.5 Percent Dextrose 5000mL (Ambu-Flex II): Recall - Presence of Particulate Matter, FDA MedWatch
• Turkish man pleads guilty to importing illegal cancer drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - July 2014 Safety Labeling Changes includes 73 products with revisions to Prescribing Information, FDA MedWatch
• Voluntary Recall Notice of McCormick Ground Oregano Due to Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 13, 2014, U.S. Food & Drug Administration (FDA)
• FDA approves Avastin to treat patients with aggressive and late-stage cervical cancer, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of efavirenz, lamivudine and tenofovir disoproxil fumarate tablets, 600 mg/300 mg/300 mg, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Enhancement Medical, Expression – Hyaluronic Acid Concentration, U.S. Food & Drug Administration (FDA)
• FDA warns consumers about fraudulent Ebola treatment products, U.S. Food & Drug Administration (FDA)
• Amgen Issues Voluntary Recall of Aranesp® (darbepoetin alfa) (500 mcg) Prefilled Syringes in Several Countries Outside of the United States Due to the Presence of Visible Particulates, U.S. Food & Drug Administration (FDA)
• Baxter Voluntarily Initiates U.S. Recall of Two Lots of Peritoneal Dialysis Solution Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA approves new type of sleep drug, Belsomra, U.S. Food & Drug Administration (FDA)
• Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution, U.S. Food & Drug Administration (FDA)
• Sunfood Recalls Organic Carob Powder Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves donor lung preservation device that may result in more lung transplants, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Wellspring Pharmaceutical Corporation, IPM Wound Gel - Microbial Contamination, U.S. Food & Drug Administration (FDA)
• August FDA Women's Health Update, FDA Office of Women's Health
• CVM Updates - FDA finds positive and negative trends in antimicrobial resistance in bacteria isolated from humans, retail meats and food animals, U.S. Food & Drug Administration (FDA)
• Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Nine Lots of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Following Complaints of Foreign Particulate Matter in Reconstituted Vials, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CUBICIN (daptomycin for injection) 500 mg in 10 mL Single Use Vials: Recall - Foreign Particulate Matter, FDA MedWatch
• FDA MedWatch - White and Blue Lion Tattoo Kits: Recall - Bacterial Contamination of Needles and Ink Bottles, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals August 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegenESlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk, U.S. Food & Drug Administration (FDA)
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  • Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegeneSlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Cubist Pharmaceuticals Issues Voluntary U.S. Recall Of Certain Lots Of CUBICIN (Daptomycin For Injection) 500 mg In 10 mL Single Use Vials Due To Presence Of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 06, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cubicin (daptomycin for injection) 500 mg in 10 mL Single Use Vials: Recall - Presence Of Particulate Matter, FDA MedWatch
• FDA MedWatch - RegenESlim Appetite Control Capsules: Recall - Presence Of DMAA, FDA MedWatch
• FDA approves Orbactiv to treat skin infections, U.S. Food & Drug Administration (FDA)
• Ortho Molecular Products Issues Allergy Alert On Undeclared Milk In Lifecore Chocolate And Lifecore Complete Chocolate, U.S. Food & Drug Administration (FDA)
• Oasis Brands, Inc Recalls Quesito Casero 12oz Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Expression Injectable by Enhancement Medical: FDA Safety Communication - Adverse Events Associated with Unapproved Use As a Dermal Filler, FDA MedWatch
• The August 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Adverse Events Associated with Use of Enhancement Medical's "Expression" Intranasal Splint as a Dermal Filler, U.S. Food & Drug Administration (FDA)
• Recomendaciones para realizar una mudanza, GobiernoUSA.gov
• New England Greens, LLC dba Vibrant Health Recalls Green Vibrance and Rainbow Vibrance Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CDPH Warns Consumers Not to Eat VR Green Farms Jarred Food Products Because of Botulism Risk, U.S. Food & Drug Administration (FDA)
• Sunburst Superfoods Recalls Organic Raw Carob Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Wawona Packing Co. Expands Its Voluntary Recall of Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA expands approval of drug to treat Pompe disease to patients of all ages; removes risk mitigation strategy requirements, U.S. Food & Drug Administration (FDA)
• FDA approves Jardiance to treat type 2 diabetes, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - August 1, 2014, U.S. Food & Drug Administration (FDA)
• Natural Grocers by Vitamin Cottage Issues Voluntary Recall For Various Chunks of Energy Products Because They Contain Organic Carob Powder From Ciranda, Inc., Which May Be Contaminated With Salmonella, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 30, 2014, U.S. Food & Drug Administration (FDA)
• FDA approves Striverdi Respimat to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
• FDA takes steps to help ensure the reliability of certain diagnostic tests, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces FY 2015 Animal Drug User Fee Rates for ADUFA and AGDUFA, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance for Industry on Cell-Based Products for Animal Use, U.S. Food & Drug Administration (FDA)
• SW Wisc Dairy Goat Products Coop issues voluntary recall of Raw Goat Milk Mild Cheddar Cheese Lot Code 103-114 because of possible health risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lidocaine HCI Injection, USP, 2 percent, by Hospira: Recall - Visible Particulates, FDA MedWatch
• Hummingbird Wholesale Recalls Organic Raw Carob Powder for Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• CONSUMER ALERT: UNDECLARED MILK IN Uprising brand Carrot Drink, Beet Drink and in Peanut Punch, U.S. Food & Drug Administration (FDA)
• Starway Inc. Issues an Alert on Undeclared Sulfites in Peony Mark Brand Roasted and Salted Pumpkin Seeds, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall Of One Lot Of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL Single-dose Vial, Preservative-free, Due To Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA Commissioner Margaret A. Hamburg’s Statement on the Surgeon General’s Call to Action to Prevent Skin Cancer, U.S. Food & Drug Administration (FDA)
• CaCoCo, Inc. Recalls Raw Drinking Chocolate Containing Voluntarily Recalled Organic Carob Powder From Their Supplier for Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• GOMACRO RECALLS "Almond Butter + Carob" and “Sunflower Butter + Chocolate” MacroBars Because of Possible Health Risk Carob Powder Supplier May Have Exposed Ingredient to Salmonella, U.S. Food & Drug Administration (FDA)
• The TJX Companies, Inc. Recalls "Ecoato" Sweet Paprika Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Carmel Food Group Announces a Voluntary Recall of One Code Date of Mislabeled Butternut Squash Ravioli Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• FDA expands approved use of Imbruvica for chronic lymphocytic leukemia, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Provides Equine Veterinarians with Important Information about TILDREN and OSPHOS for Navicular Syndrome in Horses, U.S. Food & Drug Administration (FDA)
• Dancing Star LLC, Buckland, MA 01338 Issues Voluntary Recall For Various Snacks Because They Contain Organic Carob Powder From Ciranda, Inc., Hudson, WI 54016, Which May Be Contaminated With Salmonella., U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: GE Healthcare, LLC, Single-Width Airway Modules (E-MiniC) and Accessories and Extension Modules (N-FC, N-FCREC) - CO2 Detector May Fail Leading to Injury, U.S. Food & Drug Administration (FDA)
• GE Healthcare, LLC, Single-Width Airway Modules (E-MiniC) and Accessories and Extension Modules (N-FC, N-FCREC: Class I Recall - CO2 Detector May Fail Leading to Injury, FDA MedWatch
• Texas Firm Recalls Ready-to-eat Products For Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• Lion Pavilion Issues Alert on Undeclared Sulfites in Tasty Peach Slices, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 23, 2014, U.S. Food & Drug Administration (FDA)
• Earth Circle Organics Recalls Organic Carob Powder for Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Made-In-Store Items Prepared With Stone Fruit Voluntarily Recalled by Wawona Packing Co. Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves new extended-release oxycodone with abuse-deterrent properties, U.S. Food & Drug Administration (FDA)
• FDA approves Zydelig for three types of blood cancers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ibuprofen and Oxcarbazepine Tablets by American Health Packaging: Recall - Mislabeled Packaging, FDA MedWatch
• American Health Packaging Announces the Voluntary Nationwide Recall of Ibuprofen Tablets, USP, 600 mg, 100 Hospital Unit Dose and Oxcarbazepine Tablets, 300 mg, 100 Hospital Unit Dose, U.S. Food & Drug Administration (FDA)
• Unique Pharmaceuticals, Ltd. Announces a Voluntary Nationwide Recall of all Sterile Compounded Preparations Within Their Expiry Period Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Hyannis Recalls Chocolate Chewies Cookies Due to Undeclared Tree Nut Allergen, U.S. Food & Drug Administration (FDA)
• Wegmans Issues Voluntary Recall of Bakery Products That May Contain Fresh Peaches, Nectarines and Plums Supplied by Wawona Packing Company, U.S. Food & Drug Administration (FDA)
• Wawona Packing Co. Takes Precautionary Step of Voluntarily Recalling Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Drug Products by Downing Labs (aka NuVision Pharmacy): Drug Alert - Lack of Sterility Assurance, FDA MedWatch
• Take a new CME/CNE/CPE course on the Science of Sex and Gender in Human Health, FDA Office of Women's Health