FDA News
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- Serie completa de monedas presidenciales para 2015
- FDA expands uses of Vyvanse to treat binge-eating disorder
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- United States enters consent decree prohibiting illegal distribution of Luvena Prebiotic products
- From: U.S. Food & Drug Administration (FDA)
- Spiceco Issues Allergy Alert on Undeclared Peanut Allergen in 5 Oz. Containers of Pride of Szeged Sweet Hungarian Paprika Lot # 091617PAHU05PS
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Georgia Company Recalls Certain Pecan Products Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Guidances Under Development for 2015
- From: U.S. Food & Drug Administration (FDA)
- Freeland Foods Voluntarily Recalls Sunflower Seed Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- REO Spice & Seasoning, Inc VoluntarilyRrecalls REO Country Style Chili Seasoning Due to Undeclared Peanut Allergens
- From: U.S. Food & Drug Administration (FDA)
- Aleias Gluten Free Foods, LLC Issues Allergy Alert on Undeclared Peanut Protein in Parmesan Croutons and Classic Croutons
- From: U.S. Food & Drug Administration (FDA)
- Aron Streit, Inc. Issues Allergy Alert On Undeclared Milk Allergens In "Streit's Dark Chocolate Coins"
- From: U.S. Food & Drug Administration (FDA)
- Arcadia Tradings Inc. Recalls Red Thread Fish Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- HIV/AIDS Update - Prezcobix tablet containing 800 mg of darunavir and 150 mg of cobicistat approval
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Approval of Evotaz, containing 300 mg of atazanavir and 150 mg of cobicistat
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Approval changes to the Kaletra (lopinavir/ritonavir)
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA takes steps to improve reliability of automated external defibrillators
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Dairy Recall
- From: U.S. Food & Drug Administration (FDA)
- Probar LLC Recalls Probar Base Frosted Peanut Butter Bars Due to Possible Presence of Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Lime Green Grocer, Inc. Issues Allergy Alert on Undeclared Soy in the Thai Delight Burrito
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- Infórmese sobre las drogas y el abuso de sustancias entre adolescentes
- Update of CVM's What's New - Cancellation of 2015 Windows to Regulatory Research Internship Program
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA approves first generic esomeprazole
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Comunicado Actualizado: Quesería Bendita LLC Retira Quesos Frescos Y Crema Agria Debido a Posibles Riesgos Para la Salud
- From: U.S. Food & Drug Administration (FDA)
- Dr. Robert Califf named FDA Deputy Commissioner for Medical Products and Tobacco
- From: U.S. Food & Drug Administration (FDA)
- Korean Food Co. Issues Allergy Alert on Undeclared Shrimp in Mak Kimchi
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Recalls
- From: U.S. Food & Drug Administration (FDA)
- Cox Veterinary Laboratory, Inc. Issues Voluntary Recall of “Gastroade Xtra”
- From: U.S. Food & Drug Administration (FDA)
- J.J. Fuds, Inc. Issues Recall of Pet Food Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA approves Natpara to control low blood calcium levels in patients with hypoparathyroidism
- From: U.S. Food & Drug Administration (FDA)
- FDA approves a second vaccine to prevent serogroup B meningococcal disease
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA permits marketing of first system of mobile medical apps for continuous glucose monitoring
- From: U.S. Food & Drug Administration (FDA)
- Second Turkish man sentenced for smuggling counterfeit cancer drugs
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - 0.9 Percent Sodium Chloride Injection, USP, 250 mL by Hospira : Recall - Particulate Matter
- Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 250 mL Due to Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Freeland Foods Voluntarily Recalls Spicy Seed Due To Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Gonnella Baking Company Issues Allergy Alert on Undeclared Milk in Jewel Brand Gourmet Sandwich Rolls and Gonnella Brand Sub Buns
- From: U.S. Food & Drug Administration (FDA)
- Tarrier Foods Issues Allergy Alert on Undeclared Peanuts and Egg in Chopped Twix
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Reconozca las etiquetas y los códigos de sus alimentos
- FDA MedWatch - Bone Graft Substitutes Containing Recombinant Proteins or Synthetic Peptides in Patients Under Age 18: FDA Safety Communication - Reports of Serious Injuries
- Medical Device Safety and Recalls: Use of Bone Graft Substitutes Containing Recombinant Proteins or Synthetic Peptides in Patients under Age 18 – FDA Safety Communication
- From: U.S. Food & Drug Administration (FDA)
- Northern Tier Bakery Issues Allergy Alert on Potential Undeclared Peanut in Product
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Drug Shortages 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)
- CVM Updates - New FDA Guidance Document Search Now Available
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA and Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Oma’s Pride Recalls Purr Complete Feline Poultry Meal because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- B&M, Inc. Issues Allergy Alert on Undeclared Peanut Protein in Ground Seasonings Sold at Harris Teeter in the Southeast Region Due to Potential Undeclared Peanut Protein
- From: U.S. Food & Drug Administration (FDA)
- Oma's Pride Recalls Purr Complete Feline Poultry Meal because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- B&M, Inc. Issues Allergy Allert on Undeclared Peanut Protein in Ground Cumin and Other Seasonings Sold at Target and the Fresh Market Nationwide due to Potential Undeclared Peanut Protein
- From: U.S. Food & Drug Administration (FDA)
- Inventure Foods, Inc. Issues Voluntary Recall Of Its Rader Farms Fresh Start Smoothie Blend, Sunrise Refresh Fusion, And Daily Power Fusion Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Queseria Bendita LLC Recalls Fresh Cheeses and Sour Cream Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 14, 2015
- From: U.S. Food & Drug Administration (FDA)
- Haga crecer su negocio con el Programa de Desarrollo Empresarial 8(a)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Federal judge approves consent decree with California dietary supplement maker
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Franklin Farms Issues Allergy Alert for Chili-Bean Veggiburgers Due to Undeclared Peanut Allergen
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- NAC Foods Co. Issues An Allergy Alert on Undeclared Peanut Protein on Ground Cumin Product
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Simulated IV Solutions from Wallcur: CDER Statement- FDA's Investigation into Patients being Injected
- Whole Foods Market Cranston Recalls Salted Caramel Crispies Due to Undeclared Allergen
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Conozca la diferencia entre la influenza y el ébola
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
- From: 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”
- From: 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"
- From: U.S. Food & Drug Administration (FDA)
- Zenobia Company LLC. Issues Allergy Alert on Undeclared Peanut Protein in "My Spice Sage Cumin Ground”
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Winn-Dixie Recalls Bakery Sour Cream Lemon Pies
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Bidart Bros. Works with Federal and State Officials to Determine Source of Listeriosis-Associated Outbreak
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- The Santa Barbara Smokehouse Inc Voluntary Recall Because of Possible Health Risk
- From: 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
- DICK'S Sporting Goods Voluntarily Recalls Fitness Gear Inversion Table
- From: 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
- 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)
- Update of CVM's What's New - Public Master Files (PMFs) in development updated
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 07, 2015
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 31, 2014
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Veterinary Master Files
- From: U.S. Food & Drug Administration (FDA)
- The January 2015 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals January 2015 Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Eillien's Candies Inc. Voluntarily Recalls Various Sizes and Brands of Walnut Pieces Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Happy Apple Company Expands Voluntary Recall of Caramel Apples To Include Kroger Brand Caramel Apples
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pet Treat Recalls
- From: U.S. Food & Drug Administration (FDA)
- Zilks Foods Issues Allergy Alert on Undeclared Peanuts in Hummus Products
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Asegure su futuro financiero
- Barkworthies Issues Nationwide Recall of Chicken Vittles Dog Chews
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Virazole (Ribavirin Powder For Solution) by Valeant Pharmaceutical North America, LLC: Recall- Due to Microbial Contamination
- Jump Your Bones, Inc. Recalls Roo Bites (Cubes) Pet Treats
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Adams Flavors, Foods & Ingredients Issues Allergy Alert On Undeclared Peanut Protein in Cumin Prooducts
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Halyard Health, KimVent* Microcuff* Subglottic Suctioning Endotracheal Tubes - Component May Detach During Use
- From: 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 - Nellcor Puritan Bennett 980 Ventilator System by Covidien: Class I Recall - Component Failure May Cause Burning Odor
- Medical Device Safety and Recalls: Nellcor Puritan Bennett, 980 Ventilator System
- From: 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
- From: 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
- From: 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
- From: 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
- Burkmann Feeds, Danville, KY RECALLS 656-Layer Ration 20% Pellets Because of Possible Monensin Sodium Contamination
- From: U.S. Food & Drug Administration (FDA)
- TEN BC LLC Issues Allergy Alert on Undeclared Peanuts in "Tommy’s Superfoods 10 oz. Santa Fe Rice"
- From: U.S. Food & Drug Administration (FDA)
- Great Feeling Foods, LLC Recalls Groove Gluten-Free Ice Cream Cookie Sandwiches Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Immediate Recall & Allergy Alert Undeclared Peanut Protein in Chili Mix Products
- From: U.S. Food & Drug Administration (FDA)
- Merb’s Candies Announces Voluntary Recall of Caramel Apples due to possible contamination with Listeria monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- American Roland Food Corp. Recalls Two Lots of Roland(R) Bruschetta
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 24, 2014
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Customed Inc., Surgical Convenience Packs - Compromised Sterility Due to Multiple Problems
- From: U.S. Food & Drug Administration (FDA)
- California Snack Foods Announces Recall of Karm’l Dapples/All Styles
- From: U.S. Food & Drug Administration (FDA)
- Adams Flavors, Foods & Ingredients Issues Allergy Alert On Undeclared Peanut Protein In Cumin Products
- From: U.S. Food & Drug Administration (FDA)
- Farm Country Cheese House Recalls Raw Milk Cheddar Because Of Possible Contamination With Listeria Monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Caramel Apples: Warning - Illnesses, Including Deaths, Linked to Listeria Monocytogenes Contamination
- Hospira Announces Voluntary Worldwide Recall of 10 Lots of Mitoxantrone Due to Confirmed Subpotency and Out-Of-Specification Impurities
- From: U.S. Food & Drug Administration (FDA)
- Kent, WA Firm Issues Allergy Alert on Undeclared Shellfish in Tofu Pad Thai Bowl and Thai Noodle Salad
- From: U.S. Food & Drug Administration (FDA)
- Snoqualmie Gourmet Ice Cream, Inc. Voluntarily Recalls Ice Cream, Gelato, Custard and Sorbet Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Mitoxantrone by Hospira: Recall - Confirmed Subpotency and Out-Of-Specification
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Commissioner Margaret A. Hamburg's statement on FDA’s blood donor deferral policy for men who have sex with men
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - FDA’s blood donor deferral policy for men who have sex with men
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Reily Foods Recalls Chili Seasoning Kits Due to Undeclared Peanut and Almond Allergens
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Opdivo for advanced melanoma
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Perfect Bar & Company Recalls Peanut Butter and Cranberry Crunch Nutrition Bars Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Bethel Nutritional Consulting, Inc. Issues Nationwide Voluntary Recall of SLIM-K Capsules Due to Undeclared Drug Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Kkot Saem Sprouts, Inc. Recalls Soybean Sprouts and Mungbean Sprouts Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Reily Foods Recalls Chili Seasoning Kits Due to Undeclared Peanut and Almond Allergens
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new antibacterial drug Zerbaxa
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update -
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Viekira Pak to treat hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Lynparza to treat advanced ovarian cancer
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves pathogen reduction system to treat platelets
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 17, 2014
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Relaciones Estados Unidos – Cuba: el Presidente Obama anuncia cambios
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Bleating Heart Cheese Issues Voluntary Recall of Various Cheeses Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Approval of STRIBILD efficacy supplement- NDA 203100/S-011
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Xtoro to treat swimmer’s ear
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Guía actualizada de hipotecas inversas: dos cosas que debe saber
- Guía actualizada de hipotecas inversas: dos cosas que debe saber
- Tristar Equine Issues Voluntary Recall of Gastrotec
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Tristar Equine Issues Voluntary Recall of Gastrotec
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Got a Question About Your Pet's Health?
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first pathogen reduction system to treat plasma
- From: U.S. Food & Drug Administration (FDA)
- FDA announces Pharmacy Compounding Advisory Committee members
- From: 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
- Avoid unnecessary imaging during pregnancy
- From: FDA Office of Women's Health
- Enforcement Report for December 10, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of the first newborn screening test to help detect Severe Combined Immunodeficiency
- From: U.S. Food & Drug Administration (FDA)
- FDA clears test that helps predict the risk of coronary heart disease
- From: U.S. Food & Drug Administration (FDA)
- FDA clears test that helps predict the risk of coronary heart disease
- From: FDA Office of Women's Health
- Baxter Voluntarily Initiates U.S. Recall of Two Lots of Sodium Chloride Injection, USP Due to the Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA grants CLIA waiver expanding the availability of rapid screening test for syphilis
- From: U.S. Food & Drug Administration (FDA)
- Flat Creek Farm and Dairy Recalls Cheese Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA expands approved use of Cyramza to treat aggressive non-small cell lung cancer
- From: U.S. Food & Drug Administration (FDA)
- Giant Eagle Recalls Apple Pistachio Salad With or Without Chicken Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - November 2014 Safety Labeling Changes posting includes 30 products with changes to Prescribing Information
- FDA MedWatch - Ziprasidone (Marketed as Geodon and Generics): Drug Safety Communication - Rare But Potentially Fatal Skin Reactions
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first test to confirm the presence of Human T-cell Lymphotropic Virus-I/II antibodies
- 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)
- 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
- From: U.S. Food & Drug Administration (FDA)
- Whalen’s Horseradish Products, Inc. Issues Allergy Alert on Undeclared Anchovy in Whalen’s Seafood & Burger Sauce
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Gardasil 9 for prevention of certain cancers caused by five additional types of HPV
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Import Alert for Unapproved Follicle Stimulating Hormone Drugs for Cattle
- From: U.S. Food & Drug Administration (FDA)
- ¿Tiene preguntas sobre cómo obtener cobertura médica?
- Global Garlic Inc. Recalls De Mi Pais Products Cuajada Fresca (Fresh Curd) and Cuajada Olanchana (Fresh Curd) because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Dietary Supplements Containing Live Bacteria or Yeast in Immunocompromised Persons: Warning - Risk of Invasive Fungal Disease
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- 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
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - The FDA Issues Final Guidance on Electronic Adverse Event Reporting for Animal Drugs
- From: U.S. Food & Drug Administration (FDA)
- Alere Initiates Voluntary URGENT CORRECTION for Use of Alere INRatio and INRatio2 PT/INR Monitor System
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 02, 2014
- From: U.S. Food & Drug Administration (FDA)
- Abdallah Candies Announces the Voluntary Recall of Holiday Caramel Bites
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- House of Flavors Issues Voluntary Recall Due to Possible Undeclared Dairy Allergen in Ciao Bella Dark Cocoa Sorbetto
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Lakeland Animal Nutrition Issues Voluntary Horse Feed Recall
- From: U.S. Food & Drug Administration (FDA)
- Lakeland Animal Nutrition Issues Voluntary Horse Feed Recall
- From: U.S. Food & Drug Administration (FDA)
- The December 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Jakafi to treat patients with a chronic type of bone marrow disease
- From: U.S. Food & Drug Administration (FDA)
- California seafood company to halt production until FDA documents correction of unsanitary practices
- 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)
- Medical Device Safety and Recalls: CONMED Corporation, PadPro and R2 Multi-Function Defibrillation Electrodes Will Not Work with Philips FR3 and FRx AEDs
- From: 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
- Heart Sync Inc. Issues a Voluntary Device Correction for Multi-function Defibrillation Electrodes
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Blincyto to treat a rare form of acute lymphoblastic leukemia
- From: U.S. Food & Drug Administration (FDA)
- FDA issues final rule on changes to pregnancy and lactation labeling information for prescription drug and biological products
- From: U.S. Food & Drug Administration (FDA)
- FDA issues Final Rule on Pregnancy and Lactation Labeling
- From: FDA Office of Women's Health
- Update of CVM's What's New - Animal Drug Approvals December 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Conozca los diferentes tipos de educación superior en Estados Unidos
- FDA MedWatch - Gel-E Donut and Squishon 2 Products by Children’s Medical Ventures: Recall - Potential Mold Contamination
- Medical Device Safety and Recalls: Philips / Children's Medical Ventures, Gel-E Donut and Squishon 2 - Possibility of Mold
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Siemens Healthcare Diagnostics, Rapid Gram Negative Combo Panels - May Produce Incorrect Results
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Siemens Healthcare Diagnostics, Rapid Gram Negative Combo Panels: Class I Recall - May Produce Incorrect Results
- FoodSafety.gov Recalls & Alerts Update
- Whole Foods Market West Hartford, Bishops Corner and Glastonbury Recall Tarte Aux Pommes Due to Undeclared Almonds
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - World AIDS Day
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market’s Southwest Region recalls Vegan Pumpkin Pie due to Undeclared Walnuts
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - CONMED PadPro and R2 Multi-function Defibrillation Electrodes: Device Correction - Connector Compatibility Issue With Philips FR3 and FRx Defibrillator Units
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA allows marketing of non-invasive device to help evaluate heart blood flow
- From: U.S. Food & Drug Administration (FDA)
- Select Containers of Private Selection Denali Extreme Moose Tracks Ice Cream Recalled for Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- CONMED Corporation Issues a Voluntary Device Correction for PadPro and R2 Multi-function Defibrillation Electrodes
- From: U.S. Food & Drug Administration (FDA)
- Flying Cow Creamery Voluntarily Recalls Yogurt
- From: U.S. Food & Drug Administration (FDA)
- URGENT PRODUCT RECALL NOTICE
- From: U.S. Food & Drug Administration (FDA)
- Henry’s Farm Inc. Recalls Soybean Sprouts Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - Tecfidera (dimethyl fumarate) by Biogen Idec: Drug Safety Communication - Case of Rare Brain Infection PML Reported
- Customed, Inc. Issues Recall of Sterile Convenience Kits-Trays, Bags, and New Lots Added to the Previous Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA finalizes menu and vending machine calorie labeling rules
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Natura Pet Recalls 5 Lots of Dry Cat and Dry Ferret Food due to Vitamin Insufficiency
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- UPDATED FDA Safety Communication: Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Gabapentin Capsules, USP 300 mg, by Aurobindo Pharma USA: Recall - Complaints of Empty Capsules
- FDA MedWatch - UPDATE - Laparoscopic Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication - Use Discouraged Due to Increased Risk in Women With Uterine Fibroids
- Aurobindo Pharma USA, Inc. Issues Voluntary Nationwide Recall of Northstar Label Gabapentin Capsules, USP 300 mg Due to Complaints of Empty Capsules
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - FDA launches new clinical trials demographic data page - seeking comments
- From: U.S. Food & Drug Administration (FDA)
- FDA warns against using laparoscopic power morcellators to treat uterine fibroids
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - FDA launches new clinical trials demographic data page - seeking comments
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA to Present ADUFA III Process Enhancements Live Webinar
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FDA issues additional guidance for outsourcing facilities that compound sterile human drugs
- From: U.S. Food & Drug Administration (FDA)
- FDA takes enforcement action against Michigan sandwich company
- From: U.S. Food & Drug Administration (FDA)
- Kozy Shack Enterprises, LLC Issues Allergen Alert on Unlabeled Foodservice Chocolate Pudding Cups
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled Overpouch
- Get the latest FDA News on Clinical Trials, Vaginal Microbicides, and more
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - Funding Opportunities - Minor Use/Minor Species Drug Development
- 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)
- Evershing International Trading Issues Allergy Alert on Undeclared Milk in Vinacafe Brand Coffee - Wake Up Weasel Instant Coffee mix 3-in-1
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- HIV/AIDS Update - Meeting: Blood donor deferral policy for men who have had sex with another man (MSM)
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves extended-release, single-entity hydrocodone product with abuse-deterrent properties
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Final Guidance for Microbicide Development
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur
- Enforcement Report for November 19, 2014
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- REFA Enterprises, LLC Issues Voluntary Nationwide Recall of Forever Beautiful Bee Pollen Due to Undeclared Sibutramine and Phenolphthalein
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Medical Device Safety and Recalls: Respironics California, Esprit V1000 and V200 Ventilators - Power Failure May Occur
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Recomendaciones para sus compras en temporada de fiestas
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - webinar available- 60-Day NF Qualifying (A)NADA Labeling Supplements
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Published Updated Guidance for Industry on Food Facility Registration
- From: U.S. Food & Drug Administration (FDA)
- Solgar, Inc. Issues Voluntary Class I Recall of ABC Dophilus Powder
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - ABC Dophilus Powder by Solgar, Inc: Recall - Risk of Infection
- B&G Foods Issues Allergy Alert On Undeclared Peanut And Almond In Product
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - October 2014 Safety Labeling Changes posting includes 37 products with changes to Prescribing Information
- Enforcement Report for November 12, 2014
- From: U.S. Food & Drug Administration (FDA)
- Philips Healthcare Announces Recall of Children’s Medical Ventures Gel-E Donut / Squishon 2 Products
- From: U.S. Food & Drug Administration (FDA)
- Chaotic Labz Issues Voluntary Nationwide Recall of Mayhem Dietary Supplement Due to Undeclared Dexamethasone and Cyproheptadine
- From: U.S. Food & Drug Administration (FDA)
- B&G Foods Issues Allergy Alert On Undeclared Peanut And Almond In Product
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Lundberg Family Farms Recalls Eco-Farmed and Organic Brown Rice Flour Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Solgar, Inc. Issues Voluntary Class I Recall of ABC Dophilus Powder
- From: 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
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Proper Storage of Pet Meds, Food, and Treats
- From: U.S. Food & Drug Administration (FDA)
- Talleres para pequeños negocios
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News 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)
- Inscripción en el Mercado de Seguros Médicos para el 2015
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Warning Letters for Unapproved Omeprazole Drugs Marketed for Use in Horses
- From: U.S. Food & Drug Administration (FDA)
- Día de los Veteranos - 11 de noviembre
- Update of CVM's What's New - Updated Listing of Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Marin Food Specialties, Inc. Initiates Voluntary Recall of
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - Nellcor Puritan Bennett, 980 Ventilator System: Class I Recall - Software Issue May Stop Ventilator
- Medical Device Safety and Recalls: Nellcor Puritan Bennett, 980 Ventilator System - Software Issue May Stop Ventilator
- From: U.S. Food & Drug Administration (FDA)
- Schwartz Brothers Bakery Issues Allergy Alert on Undeclared Milk in “Everything Bagels”
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News 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 - Animal Drug Approvals November 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- House of Spices (India) Inc. ISSUES ALERT ON UNDECLARED SULFITES IN “GOLDEN RAISIN”
- From: U.S. Food & Drug Administration (FDA)
- House of Spices (India) Inc. Issues Alert on Undeclared Sulfites in "Golden Raisin"
- From: U.S. Food & Drug Administration (FDA)
- Oasis Brands, Inc. Retira Productos Lacteos Santa Martha debido a Posible de Riesgos a la Salud
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 05, 2014
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA Hepatitis Update: Changes to Olysio (simeprevir) label
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Hospira, GemStar Power Supply, 3VDC
- From: 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
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- 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”
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- New Jersey Firm Issues Allergy Alert on Undeclared Fish, Wheat and Egg In Garden Rotini Salad
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Kids.gov para celebrar el Día Nacional del Niño
- Update of CVM's What's New - FDA Ensures Your Foods From Animals Are Safe
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Update of CVM's What's New - Bartlett Milling Company Issues Recall of Horse Food
- From: U.S. Food & Drug Administration (FDA)
- Bartlett Milling Company Issues Recall of Horse Food
- From: U.S. Food & Drug Administration (FDA)
- FDA Veterinarian - November 2014
- From: U.S. Food & Drug Administration (FDA)
- Marathon Ventures, Inc. Announces Voluntary Recall of Raw Macadamia Nuts Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - 10 Percent Neutral Buffered Formalin by Richard-Allan Scientific: Class I Recall - May Contain Incorrect Concentration of Formalin
- Medical Device Safety and Recalls: Richard-Allan Scientific, 10% Neutral Buffered Formalin
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 29, 2014
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Basics Webinar November 5, 2014: CVM’s Pet Food Reporting and Recall Process
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- First vaccine approved by FDA to prevent serogroup B Meningococcal disease
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Melrose Recalls Vegan Gingersnap Cookies Due to Mislabeling and Undeclared Allergens
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Shur-Green Farms Issues Voluntary Nationwide Recall of Lascadoil/Soyoil Due to Possible Lasalocid Contamination
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - Baby Wipes by Nutek Disposables, Inc.: Recall - May Contain Bacteria
- Z Natural Foods Recalls Lightly Roasted Organic Carob Powder Due to Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Rome Packing Co., Inc. Recalls Fresh And Frozen Crab Meat Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Lundberg Family Farms Recalls Sea Salt Rice Chips Due to Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- Baxter Initiates Voluntary Recall of Two Lots of Intravia Containers in the U.S. and Canada
- From: U.S. Food & Drug Administration (FDA)
- Nutek Disposables, Inc. Issues Alert Due to Potential Bacteria in Baby Wipes
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FDA MedWatch - Intravia Containers by Baxter: Recall - Particulate Matter
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new treatment for rare form of hemophilia
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 22, 2014
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Bailey Farms Inc. Recalls Fresh Serrano Chile Peppers Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA Public Meeting: Supplemental Notices of Proposed Rulemaking
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Assured Brand Naproxen Sodium Tablets by Contract Packaging Resources, Inc.: Recall - Packaging Mix-Up
- Contract Packaging Resources, Inc. Issues a Voluntary Nationwide Recall of Assured Brand Naproxen Sodium Tablets due to Packaging Mix-Up
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Covidien, Medi-Trace Cadence and Kendall Defibrillation Electrodes
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Oasis Brands, Inc. Recalls Products Lacteos Santa Martha Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Publix Issues Voluntary Recall of Publix Asian Mix
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- FoodSafety.gov Recalls & Alerts Update
- Lidocaine HCI Injection, USP 10 MG Per ML, 30 ML Single-Dose. Preservative-Free, by Hospira: Recall - Particulate Matter
- FoodSafety.gov Recalls & Alerts Update
- Cómo enviar un paquete a nuestras tropas en el extranjero
- FDA approves labeling with abuse-deterrent features for third extended-release opioid analgesic
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- New Hope Mills Issues Allergy Alert on Undeclared Soy in New Hope Mills Gluten Free Chia Pancake and Waffle Mix
- From: U.S. Food & Drug Administration (FDA)
- FDA Supports National Mammography Day
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 15, 2014
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - September 2014 Safety Labeling Changes posting includes 55 products with changes to Prescribing Information
- FDA approves Ofev to treat idiopathic pulmonary fibrosis
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Esbriet to treat idiopathic pulmonary fibrosis
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - LifeCare Flexible Intravenous Solutions by Hospira, Inc.: Recall - Potential for Leakage
- Covidien Initiates Voluntary Field Safety Alert for Medi-Trace™ Cadence and Kendall™ Multi-function Defibrillation Electrodes
- From: U.S. Food & Drug Administration (FDA)
- Sunburst Foods Recalls Products Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall Of Certain Lots of Several Lifecare Products Due To Potential For Leakage
- From: U.S. Food & Drug Administration (FDA)
- Real Foods Of Seattle, LLC Issues Allergy Alert On Undeclared Egg In Mexican Cheddar Dip
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls & Alerts Update
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA permits marketing of urinary prosthesis device for women
- From: FDA Office of Women's Health
- FDA permits marketing of urinary prosthesis device for women
- From: U.S. Food & Drug Administration (FDA)
- Real Foods Of Seattle, LLC Issues Allergy Alert On Undeclared Egg In Mexican Cheddar Dip
- California Olive And Vine Announces The Voluntary Recall Of Pumpkin Seed Pesto
- Sunburst Foods Recalls Products Because Of Possible Health Risk
- Update of CVM's What's New
- From: U.S. Food & Drug Administration (FDA)
- California Olive And Vine Announces The Voluntary Recall Of Pumpkin Seed Pesto
- From: U.S. Food & Drug Administration (FDA)
- California Firm Expands Recall of Beef Products Due To Possible Processing Flaw
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- 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 approves first combination pill to treat hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Approval of Harvoni fixed-dose combination tablet (ledipasvir and sofosbuvir) for treatment of Hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- FDA approves a new ultrasound imaging agent
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Approval of Harvoni fixed-dose combination tablet (ledipasvir and sofosbuvir) for treatment of Hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first drug-coated angioplasty balloon catheter to treat vascular disease
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Akynzeo for nausea and vomiting associated with cancer chemotherapy
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Oregon Compounding Centers, Inc. Unexpired Sterile Products: Recall - Lack of Sterility Assurance
- FDA MedWatch - ICU Medical ConMed Stat2 Flow Controller: Class 1 Recall - Delivers Higher Flow Rate than Intended
- FDA MedWatch - CareFusion EnVe and ReVel Ventilators: Class 1 Recall - Power Connection Failure
- 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert On Undelcared Eggs In Lotte Waffles
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Public Master Files (PMFs) Supporting Applications for Minor Use and Minor Species Drugs in Development
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: CareFusion 203, Inc., EnVe and ReVel ventilators - Power Connection Failure
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: ICU Medical, Inc., ConMed Stat2 Flow Controller – Delivers Higher Flow Rate than Intended
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 07, 2014
- From: U.S. Food & Drug Administration (FDA)
- Oasis Brands, Inc Recalls Cuajada en Hoja 12oz because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Oasis Brands, Inc Recalls Cuajada en Hoja 12oz because of Possible Health Risk
- FDA MedWatch - Vancomycin Hydrochloride for Injection USP, Equivalent to 1 Gram Vancomycin (Sterile Powder) by Hospira, Inc.: Recall - Uncontrolled Storage During Transit
- FDA MedWatch - SAM Junctional Tourniquet Accessory (Axilla) Strap/SAM Medical Products: Recall - Potential Clip Failure
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- 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
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Final Guidance on Terminology for Veterinary Medicinal Products Adverse Event Reporting
- From: U.S. Food & Drug Administration (FDA)
- J&b European Distribution Inc. Issues Allergy Alert For Undeclared Milk In Kupiec Rice Cakes With Dark Chocolate
- From: U.S. Food & Drug Administration (FDA)
- SAM Medical Products Implements Voluntary Recall of its Accessory (Axilla) Strap for the SAM Junctional Tourniquet
- From: U.S. Food & Drug Administration (FDA)
- HAR Maspeth Corp RECALLS Jinga brand “Pan Fried Anchovies� BECAUSE OF POSSIBLE HEALTH RISK
- From: U.S. Food & Drug Administration (FDA)
- Minnesota Firm Recalls Meat and Poultry Products for Possible Listeria Contamination
- J&b European Distribution Inc. Issues Allergy Alert For Undeclared Milk In Kupiec Rice Cakes With Dark Chocolate
- HAR Maspeth Corp RECALLS Jinga brand “Pan Fried Anchovies� BECAUSE OF POSSIBLE HEALTH RISK
- FDA MedWatch - Hudson RCI Pediatric Anesthesia Breathing Circuits by Teleflex Medical: Class I Recall - Circuit Ends May Crack or Break
- Update of CVM's What's New - Inspections, Recalls, and Other Actions with Respect to Firms that Engage in Animal Drug Compounding
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Teleflex Medical, Hudson RCI Pediatric Anesthesia Breathing Circuits
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Ketorolac Tromethamine Injection, USP, 30mg/ml by Sagent Pharmaceuticals: Recall - Incorrect Labeling
- Markpol Distributors Inc. Issues Allergy Alert on Undeclared Milk in Kupiec Rice Cakes with Dark Chocolate
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA seeks permanent injunction against Pharmaceutical Innovations, Inc.
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Veterinary Master Files
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 01, 2014
- From: U.S. Food & Drug Administration (FDA)
- The October 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Alivio tributario para sobrevivientes de ataques terroristas
- Update of CVM's What's New - Animal Drug Approvals October 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - NARMS 2011 Executive Report - Interactive Data Displays
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- IKEA Recalls PASTAÄLGAR FULLKORN And PASTAÄLGAR, Due To Non-Declared Soy Content
- From: U.S. Food & Drug Administration (FDA)
- Tropical Valley Foods Issues Allergy Alert For Potentially Undeclared Peanuts In Next By Nature Dark Chocolate Cherries
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- 3D Technologies: A New Era in Breast Cancer Detection
- From: FDA Office of Women's Health
- The FDA takes steps to strengthen cybersecurity of medical devices
- From: U.S. Food & Drug Administration (FDA)
- FDA awards grants to stimulate drug, device development for rare diseases
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Bravo Recalls Select Chicken and Turkey Pet Foods Because of Possible Salmonella Health Risk
- From: 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)
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Bedford Recalls Streusel Coffee Cake Due To Undeclared Tree Nut Allergen
- From: 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 - Xolair (omalizumab): Drug Safety Communication - Slightly Elevated Risk of Cardiovascular and Cerebrovascular Serious Adverse Events
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - Food Facility Biennial Registration Renewal
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 24, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA Office of Women's Health e-Update: September - October 2014
- From: FDA Office of Women's Health
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Approval of Vitekta
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Approval of Tybost (cobicistat) 150 mg tablets
- From: U.S. Food & Drug Administration (FDA)
- The Original Soupman Issues Allergy Alert and Recall on Certain Lots of “The Original Soupman Lobster Bisque”
- From: U.S. Food & Drug Administration (FDA)
- Gold Star Smoked Fish Corp. Voluntarily Recalls Cold Smoke Steelhead Due to Possible Listeria Monocytogenes Contamination.
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Si quiere abrir su propio negocio esta charla es para usted
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species
- From: U.S. Food & Drug Administration (FDA)
- FDA food safety challenge to spur new technologies for fighting foodborne illness
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Draft Guidance Recommending Global Standards for Bioequivalence Study
- From: U.S. Food & Drug Administration (FDA)
- Consumer Alert: Undeclared Eggs in “Coconut Bun”
- From: U.S. Food & Drug Administration (FDA)
- Glaser Organic Farms Recalls Organic Carob Powder For Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of the first test to identify five yeast pathogens directly from a blood sample
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Seeks to Make FSMA Proposals More Flexible, Targeted
- From: U.S. Food & Drug Administration (FDA)
- Celebre el Mes de la Herencia Hispana
- Enforcement Report for September 17, 2014
- From: U.S. Food & Drug Administration (FDA)
- An Alert on Uneviscerated Dried Roach (Vobla)
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Combating Antibiotic Resistance
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Research Helps Keep Animals—and People—Healthy
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Potassium Chloride Injection (Baxter): Recall - Shipping Carton Mislabeling
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- Cómo evitar la violencia juvenil en sus hijos
- Baxter Initiates U.S. Voluntary Recall of One Lot of Potassium Chloride Injection Due to Shipping Carton Mislabeling
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Mantenga la seguridad vehicular de sus niños usando el asiento correcto
- Playtex Adds Production Lot To Its March 2014 Voluntary Recall Of Certain AC/DC Power Adapters Used With the Playtex® Nurser Deluxe Double Electric Breast Pump
- From: U.S. Food & Drug Administration (FDA)
- Taylor Farms Pacific, Inc. voluntarily recalls Roma Tomatoes due to potential Salmonella contamination
- From: U.S. Food & Drug Administration (FDA)
- La nueva Guía del Consumidor ya está disponible
- FDA MedWatch - August 2014 Safety Labeling Changes posting includes 32 products with changes to Prescribing Information
- 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
- From: 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
- 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
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - OLYSIO (simeprevir) label revisions
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Conditional Approval Explained: A Resource for Veterinarians
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 10, 2014
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Publix Recalls Private Label Jalapeno Bagels
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals September 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Plum Organics Voluntarily Recalls Little Cremes Organic Rice Milk Snacks Due to Potential Choking Hazard
- From: U.S. Food & Drug Administration (FDA)
- Tullia's Recalls Sauce Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Pharmacy Creations Certain Products: Recall – Potential Non-Sterility
- Medical Device Safety and Recalls: Customed Inc., Surgical Convenience Packs - Damaged Packaging
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of the first test to assess risk of developing acute kidney injury
- From: U.S. Food & Drug Administration (FDA)
- Google reembolsará miles de dólares a usuarios de Android
- Medical Device Safety and Recalls: Cook CloverSnare 4-Loop Vascular Retrieval Snare - Snare Tip May Break During Use
- From: U.S. Food & Drug Administration (FDA)
- Tullia’s Recalls Sauce Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 03, 2014
- From: U.S. Food & Drug Administration (FDA)
- U.S. Marshals seize drug products from Flawless Beauty
- From: U.S. Food & Drug Administration (FDA)
- The September 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Keytruda for advanced melanoma
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Encuentre ayuda gratis para dejar de fumar y beber alcohol
- La Orocovena Biscuit Voluntarily Recalls Pound Cake de Queso Due to Undeclared Milk, Soy and Wheat
- From: U.S. Food & Drug Administration (FDA)
- Tjs Place recalls Basil Pesto Pasta because of potential health risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- We want to keep you updated!
- From: The HealthCare.gov Team
- FDA MedWatch - Martin Avenue Pharmacy, Inc. Compounded Sterile Preparations: Recall - Lack of Assurance of Sterility
- Martin Avenue Pharmacy, Inc. Issues a Voluntary Multi-State Recall of All Compounded Sterile Preparations Due to a Lack of Assurance of Sterility
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Dermatend Original and Dermatend Ultra: Recall - Safety Concerns
- Update of CVM's What's New - My Dog Has Cancer: What Do I Need to Know?
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - PEDIGREE® Adult Complete Nutrition Limited Recall Due to Metal Fragments
- From: U.S. Food & Drug Administration (FDA)
- PEDIGREE Adult Complete Nutrition Limited Recall Due to Metal Fragments (Expanded)
- From: U.S. Food & Drug Administration (FDA)
- Solace International, Inc. Issues Voluntary Nationwide Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Stribild labeling update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Draft Guidance Recommending Global Standard Format for Veterinary Medical Products Electronic Records
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Warning Letters for Unapproved Tear Stain Removers Used in Dogs and Cats
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 27, 2014
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Takes Steps to Strengthen Program to Assess the Safety of Chemicals in Foods, Other Products
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - DePuy Synthes Craniomaxillofacial Distraction System: Class I Recall - May Reverse Directions After Surgery
- Update of CVM's What's New - Draft Guidance for Industry Available
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Mars Petcare US Announces Voluntary Recall of 22 Bags of PEDIGREE® Brand Adult Complete Nutrition for Dogs
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: DePuy Synthes Craniomaxillofacial Distraction System - May Reverse Directions After Surgery
- From: U.S. Food & Drug Administration (FDA)
- UPDATED: CloverSnare? 4-Loop Vascular Retrieval Snare Recall
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sterile Convenience Surgical Packs by Customed, Inc.: Recall - Potential Loss of Sterility
- Customed, Inc. Issues Recall of Sterile Convenience Surgical Packs
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Approval of new fixed dose combination, TRIUMEQ (abacavir sulfate, dolutegravir, lamivudine)
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Children’s Medical Ventures Gel-E Donut and Squishon 2: Class 1 Recall - Possibility of Mold
- Labeling update for Intelence (etravirine)
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Children’s Medical Ventures, Gel-E Donut and Squishon 2 - Possibility of Mold
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 20, 2014
- From: 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
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
- From: 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
- From: 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
- Medical Device Safety and Recalls: Cardiovascular Systems Diamondback 360 Peripheral Orbital Atherectomy System
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Conozca los programas escolares de nutrición infantil
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- 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
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Turkish man pleads guilty to importing illegal cancer drugs
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - July 2014 Safety Labeling Changes includes 73 products with revisions to Prescribing Information
- Voluntary Recall Notice of McCormick Ground Oregano Due to Possible Salmonella Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 13, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Avastin to treat patients with aggressive and late-stage cervical cancer
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Enhancement Medical, Expression – Hyaluronic Acid Concentration
- From: U.S. Food & Drug Administration (FDA)
- FDA warns consumers about fraudulent Ebola treatment products
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new type of sleep drug, Belsomra
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution
- From: U.S. Food & Drug Administration (FDA)
- Sunfood Recalls Organic Carob Powder Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA approves donor lung preservation device that may result in more lung transplants
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Wellspring Pharmaceutical Corporation, IPM Wound Gel - Microbial Contamination
- From: U.S. Food & Drug Administration (FDA)
- August FDA Women's Health Update
- From: FDA Office of Women's Health
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA finds positive and negative trends in antimicrobial resistance in bacteria isolated from humans, retail meats and food animals
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New
- From: 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
- From: 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
- From: 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 - White and Blue Lion Tattoo Kits: Recall - Bacterial Contamination of Needles and Ink Bottles
- Drug Shortages 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)
[Index of Archives]
[CDC News]
[NIH News]
[Epson Inkjet]
[Yosemite]
