FDA News Releases

• Date Index

• Food Safety Recalls & Alerts, (continued)
  • Food Safety Recalls & Alerts, FoodSafety.gov
  • Food Safety Recalls & Alerts, FoodSafety.gov
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• Federal judge approves consent decree with California dietary supplement maker, U.S. Food & Drug Administration (FDA)
• Garden Lites Issues Allergy Alert on Undeclared Peanuts in Garden Lites Kale & Quinoa Soufflé, Garden Lites Southwestern Soufflé, Garden Lites Veggie Chili & Cornbread Melt, Garden Lites Kale & Brown Rice Veggie Bites & Classic Cooking Kale and Quinoa Veggie Cakes, U.S. Food & Drug Administration (FDA)
• Franklin Farms Issues Allergy Alert for Chili-Bean Veggiburgers Due to Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• Gilster - Mary Lee Corp. Issues an Allergen Alert for Undeclared Almonds in Market Pantry Honey & Oat Mixers Ready to Eat Cereal, U.S. Food & Drug Administration (FDA)
• NAC Foods Co. Issues An Allergy Alert on Undeclared Peanut Protein on Ground Cumin Product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Simulated IV Solutions from Wallcur: CDER Statement- FDA's Investigation into Patients being Injected, FDA MedWatch
• Whole Foods Market Cranston Recalls Salted Caramel Crispies Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Condies Foods, Inc. Issues Allergy Alert on Undeclared Peanut Protein in Condies Brand “Bold And Zesty” and Dr. J’s Brand “Mild” and “Medium” Salsas, U.S. Food & Drug Administration (FDA)
• Conozca la diferencia entre la influenza y el ébola, GobiernoUSA.gov
• Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
• Spice n’ More Issues Allergy Alert on Undeclared Peanuts in Cumin Powder "Casablanca", “Salma”, “Spice Class”, “La Mina”, “Key Food” and “H Harvest”, U.S. Food & Drug Administration (FDA)
• Spice N'More Issues Allergy Alert on Undeclared Peanuts in Cumin Powder "Casablanca", "Salma", "Spice Class", "La Mina", "Leader Meret", "All Island Spice", "Key Food" and "H Harvest", U.S. Food & Drug Administration (FDA)
• Zenobia Company LLC. Issues Allergy Alert on Undeclared Peanut Protein in "My Spice Sage Cumin Ground”, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
• Taj Ethnic Gourmet® Brand Issues a Voluntary Recall for Certain Retail Lots of Indian Sauces Due to Potential Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• Winn-Dixie Recalls Bakery Sour Cream Lemon Pies, U.S. Food & Drug Administration (FDA)
• Morningstar Farms Issues Allergy Alert and Voluntary, Precautionary Recall of Spicy Black Bean Burgers and Chipotle Black Bean Burgers in The U.S. Due to Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• Bidart Bros. Works with Federal and State Officials to Determine Source of Listeriosis-Associated Outbreak, U.S. Food & Drug Administration (FDA)
• Con Yeager Spice Company Issues a Voluntary Recall for Ground Cumin and Seasoning Blends (containing Ground Cumin) Due to Potential Undeclared Peanut Allergens, U.S. Food & Drug Administration (FDA)
• Wallcur Practi-0.9% Sodium Chloride-IV Bags 50 mL, 250 mL, 500, mL, and 1000 mL Wallcur Practi-0.9% Sodium Chloride-IV Bag with Distilled Water 100 mL, U.S. Food & Drug Administration (FDA)
• The Santa Barbara Smokehouse Inc Voluntary Recall Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Prescription and Over-the-Counter (OTC) Pain Medicines: Drug Safety Communication - FDA Review of Possible Risks of Pain Medicine Use During Pregnancy, FDA MedWatch
• DICK'S Sporting Goods Voluntarily Recalls Fitness Gear Inversion Table, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Alere San Diego Inc., Alere INRatio and INRatio2 PT/INR Monitor System (Professional and Prescription Home Use) - Falsely Low INR Test Results, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Public Master Files (PMFs) in development updated, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Public Master Files (PMFs) in development updated, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Public Master Files (PMFs) in development updated, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 07, 2015, U.S. Food & Drug Administration (FDA)
• H-E-B Issues a Voluntary Precautionary Recall For Certain Single Serving Soups Due to Potential Undeclared Peanut Allergens, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 31, 2014, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
• The January 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals January 2015 Update, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Assorted Cookie Platters Sold in Arizona, Southern California, Hawaii and Nevada Due to Undeclared Nut Allergens, U.S. Food & Drug Administration (FDA)
• Eillien's Candies Inc. Voluntarily Recalls Various Sizes and Brands of Walnut Pieces Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Happy Apple Company Expands Voluntary Recall of Caramel Apples To Include Kroger Brand Caramel Apples, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Burkmann Feeds, Danville, KY Recalls 656-Layer Ration 20% Pellets Because of Possible Monensin Sodium Contamination, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pet Treat Recalls, U.S. Food & Drug Administration (FDA)
• Zilks Foods Issues Allergy Alert on Undeclared Peanuts in Hummus Products, U.S. Food & Drug Administration (FDA)
• Full Tilt Ice Cream Recalls All Dairy Based Ice Cream Products Except Non-Dairy Frozen Desserts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Asegure su futuro financiero, GobiernoUSA.gov
• Barkworthies Issues Nationwide Recall of Chicken Vittles Dog Chews, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Virazole (Ribavirin Powder For Solution) by Valeant Pharmaceutical North America, LLC: Recall- Due to Microbial Contamination, FDA MedWatch
• Jump Your Bones, Inc. Recalls Roo Bites (Cubes) Pet Treats, U.S. Food & Drug Administration (FDA)
• Valeant Pharmaceutical North America LLC Issues Voluntary Nationwide Recall Of Virazole (Ribavirin Powder For Solution) Due To Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Cut, Wrapped and Weighed Bleating Heart-Brand Cheeses in Arizona, California and Hawaii Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Adams Flavors, Foods & Ingredients Issues Allergy Alert On Undeclared Peanut Protein in Cumin Prooducts, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Halyard Health, KimVent* Microcuff* Subglottic Suctioning Endotracheal Tubes - Component May Detach During Use, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - KimVent Microcuff Subglottic Suctioning Endotracheal Tubes by Halyard Health: Class I Recall - Component May Detach During Use, FDA MedWatch
• FDA MedWatch - Nellcor Puritan Bennett 980 Ventilator System by Covidien: Class I Recall - Component Failure May Cause Burning Odor, FDA MedWatch
• Medical Device Safety and Recalls: Nellcor Puritan Bennett, 980 Ventilator System, U.S. Food & Drug Administration (FDA)
• Pink’s Ice Cream Recalls All Ice Cream Flavors Except the Coconut Non-Dairy Frozen Dessert Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• John B. Sanfilippo & Son, Inc. Voluntarily Recalls Fisher Brand 8 oz. Chopped Walnuts and Fisher Brand 8 oz. Pecan Cookie Pieces Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bleating Heart Cheese Expanding Voluntary Recall To Include All Cheese Produced Between February 14, 2014 To September 19, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - IV Solutions from Wallcur of San Diego: CDER Statement - FDA Warns Health Care Professionals Not to Inject Patients, FDA MedWatch
• Burkmann Feeds, Danville, KY RECALLS 656-Layer Ration 20% Pellets Because of Possible Monensin Sodium Contamination, U.S. Food & Drug Administration (FDA)
• TEN BC LLC Issues Allergy Alert on Undeclared Peanuts in "Tommy’s Superfoods 10 oz. Santa Fe Rice", U.S. Food & Drug Administration (FDA)
• Great Feeling Foods, LLC Recalls Groove Gluten-Free Ice Cream Cookie Sandwiches Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Immediate Recall & Allergy Alert Undeclared Peanut Protein in Chili Mix Products, U.S. Food & Drug Administration (FDA)
• Merb’s Candies Announces Voluntary Recall of Caramel Apples due to possible contamination with Listeria monocytogenes, U.S. Food & Drug Administration (FDA)
• American Roland Food Corp. Recalls Two Lots of Roland(R) Bruschetta, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 24, 2014, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Heart Sync, Multi-function Defibrillation Electrodes Will Not Work with Philips FR3 and FRx AEDs, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Customed Inc., Surgical Convenience Packs - Compromised Sterility Due to Multiple Problems, U.S. Food & Drug Administration (FDA)
• California Snack Foods Announces Recall of Karm’l Dapples/All Styles, U.S. Food & Drug Administration (FDA)
• Adams Flavors, Foods & Ingredients Issues Allergy Alert On Undeclared Peanut Protein In Cumin Products, U.S. Food & Drug Administration (FDA)
• Farm Country Cheese House Recalls Raw Milk Cheddar Because Of Possible Contamination With Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Caramel Apples: Warning - Illnesses, Including Deaths, Linked to Listeria Monocytogenes Contamination, FDA MedWatch
• Hospira Announces Voluntary Worldwide Recall of 10 Lots of Mitoxantrone Due to Confirmed Subpotency and Out-Of-Specification Impurities, U.S. Food & Drug Administration (FDA)
• Kent, WA Firm Issues Allergy Alert on Undeclared Shellfish in Tofu Pad Thai Bowl and Thai Noodle Salad, U.S. Food & Drug Administration (FDA)
• Snoqualmie Gourmet Ice Cream, Inc. Voluntarily Recalls Ice Cream, Gelato, Custard and Sorbet Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mitoxantrone by Hospira: Recall - Confirmed Subpotency and Out-Of-Specification, FDA MedWatch
• FDA Commissioner Margaret A. Hamburg's statement on FDA’s blood donor deferral policy for men who have sex with men, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - FDA’s blood donor deferral policy for men who have sex with men, U.S. Food & Drug Administration (FDA)
• FDA approves Opdivo for advanced melanoma, U.S. Food & Drug Administration (FDA)
• Perfect Bar & Company Recalls Peanut Butter and Cranberry Crunch Nutrition Bars Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bethel Nutritional Consulting, Inc. Issues Nationwide Voluntary Recall of SLIM-K Capsules Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Kkot Saem Sprouts, Inc. Recalls Soybean Sprouts and Mungbean Sprouts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bethel Nutritional Consulting, Inc. Issues Nationwide Voluntary Recall of B-Lipo Capsules Due to the Presence of an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• Reily Foods Recalls Chili Seasoning Kits Due to Undeclared Peanut and Almond Allergens, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Reily Foods Recalls Chili Seasoning Kits Due to Undeclared Peanut and Almond Allergens, U.S. Food & Drug Administration (FDA)
• FDA approves new antibacterial drug Zerbaxa, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update -, U.S. Food & Drug Administration (FDA)
• FDA approves Viekira Pak to treat hepatitis C, U.S. Food & Drug Administration (FDA)
• FDA approves Lynparza to treat advanced ovarian cancer, U.S. Food & Drug Administration (FDA)
• Zachary Confections, Inc. Announces a Nationwide Voluntary Recall of Market Pantry (Target) Dark Chocolate Covered Almonds For Undeclared Peanut in Product, U.S. Food & Drug Administration (FDA)
• FDA approves pathogen reduction system to treat platelets, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 17, 2014, U.S. Food & Drug Administration (FDA)
• Relaciones Estados Unidos – Cuba: el Presidente Obama anuncia cambios, GobiernoUSA.gov
• Bleating Heart Cheese Issues Voluntary Recall of Various Cheeses Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Approval of STRIBILD efficacy supplement- NDA 203100/S-011, U.S. Food & Drug Administration (FDA)
• FDA approves Xtoro to treat swimmer’s ear, U.S. Food & Drug Administration (FDA)
• Guía actualizada de hipotecas inversas: dos cosas que debe saber, GobiernoUSA.gov
  • <Possible follow-ups>
  • Guía actualizada de hipotecas inversas: dos cosas que debe saber, GobiernoUSA.gov
• Tristar Equine Issues Voluntary Recall of Gastrotec, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Tristar Equine Issues Voluntary Recall of Gastrotec, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Got a Question About Your Pet's Health?, U.S. Food & Drug Administration (FDA)
• FDA approves first pathogen reduction system to treat plasma, U.S. Food & Drug Administration (FDA)
• FDA announces Pharmacy Compounding Advisory Committee members, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter, FDA MedWatch
• Avoid unnecessary imaging during pregnancy, FDA Office of Women's Health
• Enforcement Report for December 10, 2014, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of the first newborn screening test to help detect Severe Combined Immunodeficiency, U.S. Food & Drug Administration (FDA)
• FDA clears test that helps predict the risk of coronary heart disease, FDA Office of Women's Health
  • <Possible follow-ups>
  • FDA clears test that helps predict the risk of coronary heart disease, U.S. Food & Drug Administration (FDA)
• Baxter Voluntarily Initiates U.S. Recall of Two Lots of Sodium Chloride Injection, USP Due to the Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA grants CLIA waiver expanding the availability of rapid screening test for syphilis, U.S. Food & Drug Administration (FDA)
• Flat Creek Farm and Dairy Recalls Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA expands approved use of Cyramza to treat aggressive non-small cell lung cancer, U.S. Food & Drug Administration (FDA)
• Giant Eagle Recalls Apple Pistachio Salad With or Without Chicken Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2014 Safety Labeling Changes posting includes 30 products with changes to Prescribing Information, FDA MedWatch
• FDA MedWatch - Ziprasidone (Marketed as Geodon and Generics): Drug Safety Communication - Rare But Potentially Fatal Skin Reactions, FDA MedWatch
• FDA approves first test to confirm the presence of Human T-cell Lymphotropic Virus-I/II antibodies, U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Produce N.A., Inc. Voluntarily Recalls Fresh Cut Fruit Containing Gala Red Apple in a Few States in North East US Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whalen’s Horseradish Products, Inc. Issues Allergy Alert on Undeclared Anchovy in Whalen’s Seafood & Burger Sauce, U.S. Food & Drug Administration (FDA)
• FDA approves Gardasil 9 for prevention of certain cancers caused by five additional types of HPV, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Import Alert for Unapproved Follicle Stimulating Hormone Drugs for Cattle, U.S. Food & Drug Administration (FDA)
• ¿Tiene preguntas sobre cómo obtener cobertura médica?, GobiernoUSA.gov
• Global Garlic Inc. Recalls De Mi Pais Products Cuajada Fresca (Fresh Curd) and Cuajada Olanchana (Fresh Curd) because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Dietary Supplements Containing Live Bacteria or Yeast in Immunocompromised Persons: Warning - Risk of Invasive Fungal Disease, FDA MedWatch
• FDA MedWatch - Alere INRatio2 PT/INR Professional Test Strips: UPDATE - Significant Discrepancy in INR Results May Lead To a Delay In An Urgent Medical Decision, FDA MedWatch
• CVM Updates - The FDA Issues Final Guidance on Electronic Adverse Event Reporting for Animal Drugs, U.S. Food & Drug Administration (FDA)
• Alere Initiates Voluntary URGENT CORRECTION for Use of Alere INRatio and INRatio2 PT/INR Monitor System, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 02, 2014, U.S. Food & Drug Administration (FDA)
• Abdallah Candies Announces the Voluntary Recall of Holiday Caramel Bites, U.S. Food & Drug Administration (FDA)
• Safeway Recalls Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream Sold November 4 through December 5 Due to an Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• House of Flavors Issues Voluntary Recall Due to Possible Undeclared Dairy Allergen in Ciao Bella Dark Cocoa Sorbetto, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Lakeland Animal Nutrition Issues Voluntary Horse Feed Recall, U.S. Food & Drug Administration (FDA)
• Lakeland Animal Nutrition Issues Voluntary Horse Feed Recall, U.S. Food & Drug Administration (FDA)
• The December 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Overhill Farms Voluntarily Recalls Open Nature Chile Cheese Enchiladas Sold At Safeway Stores Nationwide Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA approves Jakafi to treat patients with a chronic type of bone marrow disease, U.S. Food & Drug Administration (FDA)
• California seafood company to halt production until FDA documents correction of unsanitary practices, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: CONMED Corporation, PadPro and R2 Multi-Function Defibrillation Electrodes Will Not Work with Philips FR3 and FRx AEDs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heart Sync Inc. Multi-function Defibrillation Electrodes: Device Correction - Connector Incompatibility with Philips FR3 and FRx Defibrillator Units, FDA MedWatch
• Heart Sync Inc. Issues a Voluntary Device Correction for Multi-function Defibrillation Electrodes, U.S. Food & Drug Administration (FDA)
• FDA approves Blincyto to treat a rare form of acute lymphoblastic leukemia, U.S. Food & Drug Administration (FDA)
• FDA issues final rule on changes to pregnancy and lactation labeling information for prescription drug and biological products, U.S. Food & Drug Administration (FDA)
• FDA issues Final Rule on Pregnancy and Lactation Labeling, FDA Office of Women's Health
• Update of CVM's What's New - Animal Drug Approvals December 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Conozca los diferentes tipos de educación superior en Estados Unidos, GobiernoUSA.gov
• FDA MedWatch - Gel-E Donut and Squishon 2 Products by Children’s Medical Ventures: Recall - Potential Mold Contamination, FDA MedWatch
• Medical Device Safety and Recalls: Philips / Children's Medical Ventures, Gel-E Donut and Squishon 2 - Possibility of Mold, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Siemens Healthcare Diagnostics, Rapid Gram Negative Combo Panels - May Produce Incorrect Results, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Siemens Healthcare Diagnostics, Rapid Gram Negative Combo Panels: Class I Recall - May Produce Incorrect Results, FDA MedWatch
• Whole Foods Market West Hartford, Bishops Corner and Glastonbury Recall Tarte Aux Pommes Due to Undeclared Almonds, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - World AIDS Day, U.S. Food & Drug Administration (FDA)
• Whole Foods Market’s Southwest Region recalls Vegan Pumpkin Pie due to Undeclared Walnuts, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CONMED PadPro and R2 Multi-function Defibrillation Electrodes: Device Correction - Connector Compatibility Issue With Philips FR3 and FRx Defibrillator Units, FDA MedWatch
• FDA allows marketing of non-invasive device to help evaluate heart blood flow, U.S. Food & Drug Administration (FDA)
• Select Containers of Private Selection Denali Extreme Moose Tracks Ice Cream Recalled for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• CONMED Corporation Issues a Voluntary Device Correction for PadPro and R2 Multi-function Defibrillation Electrodes, U.S. Food & Drug Administration (FDA)
• Flying Cow Creamery Voluntarily Recalls Yogurt, U.S. Food & Drug Administration (FDA)
• URGENT PRODUCT RECALL NOTICE, U.S. Food & Drug Administration (FDA)
• Henry’s Farm Inc. Recalls Soybean Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tecfidera (dimethyl fumarate) by Biogen Idec: Drug Safety Communication - Case of Rare Brain Infection PML Reported, FDA MedWatch
• Customed, Inc. Issues Recall of Sterile Convenience Kits-Trays, Bags, and New Lots Added to the Previous Recall, U.S. Food & Drug Administration (FDA)
• FDA finalizes menu and vending machine calorie labeling rules, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natura Pet Recalls 5 Lots of Dry Cat and Dry Ferret Food due to Vitamin Insufficiency, U.S. Food & Drug Administration (FDA)
• Natura Pet Recalls 5 Lots of Dry Cat and Dry Ferret Food due to Vitamin Insufficiency, U.S. Food & Drug Administration (FDA)
• UPDATED FDA Safety Communication: Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Gabapentin Capsules, USP 300 mg, by Aurobindo Pharma USA: Recall - Complaints of Empty Capsules, FDA MedWatch
• FDA MedWatch - UPDATE - Laparoscopic Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication - Use Discouraged Due to Increased Risk in Women With Uterine Fibroids, FDA MedWatch
• Aurobindo Pharma USA, Inc. Issues Voluntary Nationwide Recall of Northstar Label Gabapentin Capsules, USP 300 mg Due to Complaints of Empty Capsules, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA launches new clinical trials demographic data page - seeking comments, U.S. Food & Drug Administration (FDA)
• FDA warns against using laparoscopic power morcellators to treat uterine fibroids, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - FDA launches new clinical trials demographic data page - seeking comments, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA to Present ADUFA III Process Enhancements Live Webinar, U.S. Food & Drug Administration (FDA)
• FDA issues additional guidance for outsourcing facilities that compound sterile human drugs, U.S. Food & Drug Administration (FDA)
• FDA takes enforcement action against Michigan sandwich company, U.S. Food & Drug Administration (FDA)
• Kozy Shack Enterprises, LLC Issues Allergen Alert on Unlabeled Foodservice Chocolate Pudding Cups, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled Overpouch, FDA MedWatch
• Get the latest FDA News on Clinical Trials, Vaginal Microbicides, and more, U.S. Food & Drug Administration (FDA)
• Baxter Initiate Voluntary Recall of One Lot of Highly COncentrated Potassium Chloride Injection In The U.S. Due to Mislabeled Overpouch, U.S. Food & Drug Administration (FDA)
• CVM Updates - Funding Opportunities - Minor Use/Minor Species Drug Development, U.S. Food & Drug Administration (FDA)
• Evershing International Trading Issues Allergy Alert on Undeclared Milk in Vinacafe Brand Coffee - Wake Up Weasel Instant Coffee mix 3-in-1, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Meeting: Blood donor deferral policy for men who have had sex with another man (MSM), U.S. Food & Drug Administration (FDA)
• FDA approves extended-release, single-entity hydrocodone product with abuse-deterrent properties, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Final Guidance for Microbicide Development, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baxter Healthcare Corporation, INTRAVIA Empty Containers with PVC Ports – Particles Found in Patient Solution, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur, FDA MedWatch
• Enforcement Report for November 19, 2014, U.S. Food & Drug Administration (FDA)
• REFA Enterprises, LLC Issues Voluntary Nationwide Recall of Forever Beautiful Bee Pollen Due to Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Respironics California, Esprit V1000 and V200 Ventilators - Power Failure May Occur, U.S. Food & Drug Administration (FDA)
• Recomendaciones para sus compras en temporada de fiestas, GobiernoUSA.gov
• Update of CVM's What's New - webinar available- 60-Day NF Qualifying (A)NADA Labeling Supplements, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Published Updated Guidance for Industry on Food Facility Registration, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ABC Dophilus Powder by Solgar, Inc: Recall - Risk of Infection, FDA MedWatch
• FDA MedWatch - October 2014 Safety Labeling Changes posting includes 37 products with changes to Prescribing Information, FDA MedWatch
• Enforcement Report for November 12, 2014, U.S. Food & Drug Administration (FDA)
• Philips Healthcare Announces Recall of Children’s Medical Ventures Gel-E Donut / Squishon 2 Products, U.S. Food & Drug Administration (FDA)
• Chaotic Labz Issues Voluntary Nationwide Recall of Mayhem Dietary Supplement Due to Undeclared Dexamethasone and Cyproheptadine, U.S. Food & Drug Administration (FDA)
• B&G Foods Issues Allergy Alert On Undeclared Peanut And Almond In Product, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • B&G Foods Issues Allergy Alert On Undeclared Peanut And Almond In Product, U.S. Food & Drug Administration (FDA)
• Great American Appetizers, Inc. Recalls Hyvee Mozzarella Cheese Sticks Due To Undeclared Soy Flour, Yellow #5, And Yellow #6, U.S. Food & Drug Administration (FDA)
• Lundberg Family Farms Recalls Eco-Farmed and Organic Brown Rice Flour Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Solgar, Inc. Issues Voluntary Class I Recall of ABC Dophilus Powder, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Solgar, Inc. Issues Voluntary Class I Recall of ABC Dophilus Powder, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Long-term Antiplatelet Therapy: Safety Announcement - Preliminary Trial Data Shows Benefits But a Higher Risk of Non-Cardiovascular Death, FDA MedWatch
• Update of CVM's What's New - Proper Storage of Pet Meds, Food, and Treats, U.S. Food & Drug Administration (FDA)
• Talleres para pequeños negocios, GobiernoUSA.gov
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
• Inscripción en el Mercado de Seguros Médicos para el 2015, GobiernoUSA.gov
• CVM Updates - FDA Issues Warning Letters for Unapproved Omeprazole Drugs Marketed for Use in Horses, U.S. Food & Drug Administration (FDA)
• Día de los Veteranos - 11 de noviembre, GobiernoUSA.gov
• Update of CVM's What's New - Updated Listing of Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Listing of Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses, U.S. Food & Drug Administration (FDA)
• Marin Food Specialties, Inc. Initiates Voluntary Recall of, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nellcor Puritan Bennett, 980 Ventilator System: Class I Recall - Software Issue May Stop Ventilator, FDA MedWatch
• Medical Device Safety and Recalls: Nellcor Puritan Bennett, 980 Ventilator System - Software Issue May Stop Ventilator, U.S. Food & Drug Administration (FDA)
• Schwartz Brothers Bakery Issues Allergy Alert on Undeclared Milk in “Everything Bagels”, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • 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)
  • 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)
  • 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)
  • 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)
  • 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)
  • 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)
  • 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)
  • 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)