FDA News Releases

• Date Index

• FDA MedWatch - Anticoagulant Citrate Phosphate Dextrose Solution, USP (CPD) BLOOD-PACK Unit By Fenwal: Recall - Labeling Issue Identified, FDA MedWatch
• FDA approves Plan B One-Step emergency contraceptive without a prescription for women 15 years of age and older, U.S. Food & Drug Administration (FDA)
• Done vida: inscríbase en su estado, GobiernoUSA.gov
• FDA MedWatch - Samsca (Tolvaptan): Drug Safety Communication - FDA Limits Duration and Usage Due To Possible Liver Injury Leading to Organ Transplant or Death, FDA MedWatch
• FDA MedWatch - Piperacillin and Tazobactam for Injection, USP 40.5 grams: Recall - Precipitation or Crystallization in IV Bag or IV Line Upon Reconstitution, FDA MedWatch
• Update of CVM's What's New - Updated Listing of Medicated Feed Mill Licenses/Veterinary Feed Directive Distributors, U.S. Food & Drug Administration (FDA)
• Sirven comidas nutritivas durante el verano a niños que las necesitan, GobiernoUSA.gov
• Voluntary Nationwide Recall of 15 Lots of Piperacillin and Tazobactam for Injection, USP 40.5 Grams Due to Possibility of Precipitation / Crystallization in IV Bag or IV Line Upon Reconstitution, U.S. Food & Drug Administration (FDA)
• Smart & Final issues Recall - Allergy Alert Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini, U.S. Food & Drug Administration (FDA)
• FDA approves Kcentra for the urgent reversal of anticoagulation in adults with major bleeding, U.S. Food & Drug Administration (FDA)
• Proteja a su bebé de infecciones, GobiernoUSA.gov
• Maple View Farm Recalls Three Flavors of Ice Cream Because of Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Inc., GemStar Infusion System: Recall - Lithium Battery Low Voltage, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot Of 0.9% Sodium Chloride Injection, Usp, 100 Ml, Flexible Containers Due to Particulate – Revised to Update Stericycle Phone Number, U.S. Food & Drug Administration (FDA)
• Orville Redenbacher’s® Classic Kettle Korn Ready-to-eat Popcorn Recalled Due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Únase a la charla sobre salud de las minorías, GobiernoUSA.gov
• FDA MedWatch - Potiga (Ezogabine): Drug Safety Communication - Linked To Retinal Abnormalities And Blue Skin Discoloration, FDA MedWatch
• FDA MedWatch - Eba Multivitamin Supplement By Saratoga Therapeutics LLC: Recall - Allergy Alert On Undeclared Milk Components, FDA MedWatch
• Saratoga Therapeutics, LLC Issues Allergy Alert on Undeclared Milk Components in Eba Multivitamin Supplement, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Chloride Injection 0.9 percent USP, 100 mL Flexible Containers by Hospira: Recall - Particulate Matter, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 100 ML, Flexible Containers Due to Particulate, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Changes to label for Atripla (efavirenz/emtricitabine/tenofovir disoproxil fumarate) tablets, U.S. Food & Drug Administration (FDA)
• Potential for Delivery System Catheter Separation Prompts Cook Medical to Initiate Voluntary Global Recall of Zilver® PTX® Drug Eluting Stent, U.S. Food & Drug Administration (FDA)
• Prevenga el maltrato infantil, GobiernoUSA.gov
  • <Possible follow-ups>
  • Prevenga el maltrato infantil, GobiernoUSA.gov
• HIV/AIDS Update- Prezista (darunavir) labeling changes, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 24, 2013, U.S. Food & Drug Administration (FDA)
• ¡Cuidado con el "desafío de la canela"!, GobiernoUSA.gov
• 7th Heaven Bakeries Issues Allergy Alert on Undeclared Egg, Soy And Milk in Oatmeal Raisin Cookies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare, Giraffe OmniBed and Giraffe Incubator: Class I Recall - Device May Randomly Delete Stored Information When Powered On, FDA MedWatch
• App IRS2Go, ahora en español, GobiernoUSA.gov
• FDA MedWatch - LifeScan, Inc.OneTouch Verio IQ Blood Glucose Meter - Recall: Failure to provide a warning at extremely high blood glucose levels, FDA MedWatch
• FDA MedWatch - All Sterile Compounded Products by Nora Apothecary And Alternative Therapies: Recall - Lack of Sterility Assurance, FDA MedWatch
• Nationwide Voluntary Field Correction Action Issued for GE Healthcare’s Giraffe Incubator and Giraffe OmniBed with Servo Oxygen Control System, U.S. Food & Drug Administration (FDA)
• Nora Apothecary & Alternative Therapies Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CareFusion Alaris PC Unit with Software V9.12: Class 1 Recall - Communication Error When Attached to EtCO2 or SpO2 Modules, FDA MedWatch
• Go Max Go Foods LLC Issues Voluntary Withdrawal of Snap!, Cleo's, Jokerz, Twilight, Buccaneer, Thumbs Up and Mahalo Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ¿Tiene preguntas sobre hipertensión?, GobiernoUSA.gov
• Update of CVM's What's New - FDA Announces Data Quality Webinar Related to 2008 ADUFA Reauthorization, U.S. Food & Drug Administration (FDA)
• Día del Planeta Tierra, GobiernoUSA.gov
• FDA MedWatch - Balanced Solutions All Sterile Compounded Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• CVM Updates - FDA Cautions in Interpretation of Antimicrobial Resistance Data, U.S. Food & Drug Administration (FDA)
• Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Merit Bird Company, LLS Recalls Vitae Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Merit Bird Company, LLS Recalls Vitae Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medical Bed Mattresses: FDA Safety Communication - Damaged or Worn Covers Pose Risk of Contamination and Infection, FDA MedWatch
• Update of CVM's What's New - CVM Issues Two Field Assignment, U.S. Food & Drug Administration (FDA)
• Covidien Issues Voluntary Recall of Power Pac Batteries for Newport™ HT70 and HT70 Plus Ventilators, U.S. Food & Drug Administration (FDA)
• Sus documentos vitales cuando los necesite, GobiernoUSA.gov
• Prime Food USA Issues an Alert On Listeria in Latis Brand Herring Fillet “Matiej”, Salmon Fillet Slices and Herring Fillet “Forelka” in Oil, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 17, 2013, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Changes to label for Atripla (efavirenz/emtricitabine/tenofovir disoproxil fumarate) tablets, U.S. Food & Drug Administration (FDA)
• Conozca más sobre el autismo, GobiernoUSA.gov
• Abbott Initiates Voluntary Recall of FreeStyle lnsulinx® Blood Glucose Meters in the United States, U.S. Food & Drug Administration (FDA)
• Cómo reportar información relacionada a las explosiones en Boston, GobiernoUSA.gov
• Wegmans Food Markets Announces Voluntary Recall of Select Wegmans Food You Feel Good About Roasted Red Pepper Dip, 8 oz., Due to Undeclared Milk and Eggs, U.S. Food & Drug Administration (FDA)
• FDA approves abuse-deterrent labeling for reformulated OxyContin, U.S. Food & Drug Administration (FDA)
• Cedarlane Natural Foods, Inc. Issues Allergy Allert and Voluntary Recall on O Organics Black Bean Enchiladas 9 Oz Due to Mislabeling and Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Plantar un jardín es una buena actividad familiar, GobiernoUSA.gov
• Ayude a su hijo a llevar una vida más sana, GobiernoUSA.gov
• Winn-Dixie Issues Recall On Winn-Dixie Organic 100% Apple Juice, FoodSafety.gov
• FDA MedWatch - Sterile Products Compounded, Repackaged, and Distributed by ApothéCure: Recall - Sterility Assurance Concerns, FDA MedWatch
• FDA MedWatch - Lyophilized Products Compounded by NuVision Pharmacy: Recall - Sterility Assurance Concerns, FDA MedWatch
• CVM Updates - Court Suspends Approval of Enroflox 100 for Cattle, U.S. Food & Drug Administration (FDA)
• ApothéCure, Inc. Announces Voluntary Nationwide Recall of All Lots of All Sterile Products Compounded, Repackaged, and Distributed by ApothéCure, Inc. Due to Sterility Assurance Concerns, U.S. Food & Drug Administration (FDA)
• NuVision Pharmacy Announces Voluntary Nationwide Recall of All Lots of All Lyophilized Products Compounded by NuVision Pharmacy Due to Sterility Assurance Concerns, U.S. Food & Drug Administration (FDA)
• Winn-Dixie Issues Voluntary Recall On Winn-Dixie Organic 100% Apple Juice, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2013 Safety Labeling Changes includes 53 products with revisions to Prescribing Information, FDA MedWatch
• Medicines in My Home Update: Safe Disposal of Fentanyl Transdermal System “Patches”, U.S. Food & Drug Administration (FDA)
• RECALL: Louisiana Firm Expands Recall of Cooked Meat, Poultry, and Deli Products Due To Listeria, FoodSafety.gov
• ALLERGY ALERT: Wild Blue Yonder Foods issues Recall due to Undeclared Almonds, FoodSafety.gov
• ¿Tiene preguntas sobre temas ambientales?, GobiernoUSA.gov
• Wild Blue Yonder Foods issues Recall-Allergy Alert- Undeclared Almonds in Chappaqua Crunch GF Simply Granola with Flax and Fruit, U.S. Food & Drug Administration (FDA)
• FDA Classifies Voluntary Shapematch® Cutting Guides Recall as Class I Recall, U.S. Food & Drug Administration (FDA)
• Green Valley Drugs Announces Voluntary Nationwide Recall of All Lots of All Sterile Products Compounded, Repackaged, and Distributed by Green Valley Drugs Due to Quality Control Concerns, U.S. Food & Drug Administration (FDA)
• Affirm XL, Inc Issues a Voluntary Nationwide Recall of Affirm XL Dietary Supplement Tablet, Lot 1190001 Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 10, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Green Valley Drugs: Recall of All Lots of All Sterile Products - Quality Control Concerns, FDA MedWatch
• Impuestos: sugerencias para el último minuto, GobiernoUSA.gov
• Donar vida: una opción a considerar, GobiernoUSA.gov
• Update of CVM's What's New - FDA budget requests $4.7 billion to ensure safety of food supply and to modernize medical product safety, U.S. Food & Drug Administration (FDA)
• FDA budget requests $4.7 billion to ensure safety of food supply and to modernize medical product safety, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Helpful Information for Veterinarians – Antiparasitic Resistance in Cattle and Small Ruminants in the United States, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Voice – Leave the Chocolate Out of Rover’s Celebrations, U.S. Food & Drug Administration (FDA)
• La trata de personas es una forma moderna de esclavitud, GobiernoUSA.gov
• Ley de Cuidado de Salud y su cobertura médica, GobiernoUSA.gov
• FDA MedWatch - BCI Remote Alarm Cables By Smith's Medical ASD, Inc.: Class 1 Recall - Cables Are Not Transferring Alarms, FDA MedWatch
• Ojo con las estafas tributarias más comunes, GobiernoUSA.gov
• Consumer Concepts Issues a Voluntary Nationwide Recall of ROCK-IT MAN All Natural Male Supplement Products Marketed as Dietary Supplements to Support Male Sexual Performance Due to Undeclared Active Ingredient, U.S. Food & Drug Administration (FDA)
• The April 2013 MedSun Newsletter is now available..., 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)
• La adicción a las drogas o el alcohol es una enfermedad, GobiernoUSA.gov
• Update of CVM's What's New - Veterinary Oversight of Antimicrobial Use in Livestock; Public Meetings Agenda, U.S. Food & Drug Administration (FDA)
• Centerville Pie Company Issues Allergy Alert on Undeclared (Anchovies) Fish in Clam Pies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Animas Corporation 2020 Insulin Infusion Pump: Class I Recall - False Alarm or Warning Sound, FDA MedWatch
• FDA MedWatch - BIVIGAM Immune Globulin Intravenous (Human), 10 Percent Liquid, 100 mL Sterile Vial: Recall - Visible Particles Observed, FDA MedWatch
• Little Mermaid Smoke House Recalls Smoked Herring and Pickled Herring Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Se vence el plazo para pagar los impuestos, GobiernoUSA.gov
  • <Possible follow-ups>
  • Se vence el plazo para pagar los impuestos, GobiernoUSA.gov
• Rich Products Corporation Expands Voluntary Recall to All Products Produced at Its Waycross, Georgia Facility Due to Possible Contamination with E. Coli O121, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo! Issues a Voluntary Recall for Three Raw Frozen Food Diet for Dogs and Cats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Bravo! Issues a Voluntary Recall for Three Raw Frozen Food Diet for Dogs and Cats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 03, 2013, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval: efavirenz, emtricitabine and tenofovir Disoproxil fumarate tablets, 600 mg/200 mg/300 mg, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals April 2013 Update, U.S. Food & Drug Administration (FDA)
• ¿Ya presentó su declaración de impuestos?, GobiernoUSA.gov
  • <Possible follow-ups>
  • ¿Ya presentó su declaración de impuestos?, GobiernoUSA.gov
• Cómo lidiar con las alergias de niños en primavera, GobiernoUSA.gov
• Pilot Projects Report Comment Period Extended until July 3, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Chloride Injection, 0.9 percent, 1000 mL, Flexible Container: Recall - Brass Particulates, FDA MedWatch
• Update of CVM's What's New - Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to Brass Particulates, U.S. Food & Drug Administration (FDA)
• Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Invokana to treat type 2 diabetes, U.S. Food & Drug Administration (FDA)
• Rich Products Corporation Announces a Voluntary Recall of Farm Rich® Mini Quesadillas, Farm Rich® Mini Pizza Slices, Farm Rich® Philly Cheese Steaks, Farm Rich® Mozzarella Bites, and Market Day® Mozzarella Bites Due to Possible Contamination with E. Coli O121, U.S. Food & Drug Administration (FDA)
• Lisy Corporation Issues Voluntary Recall on Undeclared Soy in 5 Seasoning Blends, U.S. Food & Drug Administration (FDA)
• Lifestyle Evolution Inc. (LEI), Issues Allergy Alert -- -Undeclared Milk in Lifestyle Evolution Inc.’s, NuGO FREE, NuGO Dark and NuGO Slim Non Dairy bars, U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Publix Deli Tri Fruit and Grain Salad, U.S. Food & Drug Administration (FDA)
• Urgent-Heartland Gourmet, LLC issues Allergy Alert on Undeclared Milk in Gluten Free Baking Mixes, U.S. Food & Drug Administration (FDA)
• Food Product Recall by the Gift Shop at Buffalo Trace Distillery Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 27, 2013, U.S. Food & Drug Administration (FDA)
• FDA approves new multiple sclerosis treatment: Tecfidera, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vascular Solutions Inc., Guardian II and Guardian II NC Hemostasis Valves: Class I Recall - Risk of Air Being Introduced Into Device, FDA MedWatch
• FDA MedWatch - Palimed Solutions, Inc. Sterile Compound Products: Recall - Visible Particulates Observed, FDA MedWatch
• La Preferida, Inc. Issues A Voluntary Recall Of La Spanish Version - Preferida Whole Pinto Beans 29 OZ. (Water & Salt), U.S. Food & Drug Administration (FDA)
• Pallimed Solutions, Inc. Announces Voluntary Nationwide Recall of All Sterile Compounded Products Dispensed, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Spacelabs Anesthesia Workstations and Service Kits: Class 1 Recall - Defect in CAS I/II Absorbers, FDA MedWatch
• FDA approves TOBI Podhaler to treat a type of bacterial lung infection in cystic fibrosis patients, U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Looking Forward and Expanding Access, Health Insurance Marketplace
• Update of CVM's What's New - Jones Natural Chews Co Recalls Woofers Dog Treats Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA issues proposal to improve the quality of automated external defibrillators, U.S. Food & Drug Administration (FDA)
• Servicios para personas con discapacidades, en GobiernoUSA.gov, GobiernoUSA.gov
• Affordable Care Act at 3: Increased Savings for Seniors, Health Insurance Marketplace
• FDA MedWatch - Clinical Specialties Compounding Pharmacy Products: Recall - All Sterile Products Recalled Due To Lack of Sterility Assurance, FDA MedWatch
• La Preferida, Inc. Issues A Voluntary Recall Of La Preferida Whole Pinto Beans 29 OZ. (Water & Salt), U.S. Food & Drug Administration (FDA)
• New Chapter, Inc. Issues Voluntary Recall Undeclared soy identified in one lot of Probiotic Elderberry dietary supplement, U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of All Compounded Products Due To Potential Mold Contamination -2, U.S. Food & Drug Administration (FDA)
• Clinical Specialties Compounding Pharmacy Announces Voluntary Nationwide Recall of All lots of Sterile Products Repackaged and Distributed by Clinical Specialties Compounding Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 20, 2013, U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Paying for Quality Saves Health Care Dollars, Health Insurance Marketplace
• FDA MedWatch - Avastin Unit Dose Syringes by Clinical Specialties: Recall - Potential For Serious Eye Infection, FDA MedWatch
• Daesang Issues Allergy Alert on Undeclared Peanuts in Mixed Soy Bean Paste (Sesame and Garlic), U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Holding Insurance Companies Accountable, Health Insurance Marketplace
• Affordable Care Act at 3: Abby's Story, Health Insurance Marketplace
• Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers Not to Eat Certain ProtiDiet High Protein Chocolate Dream Bars Manufactured by Pro-Amino International, Inc., Quebec, Canada, U.S. Food & Drug Administration (FDA)
• Clinical Specialties Issues Voluntary Nationwide Recall of Avastin Unit Dose Syringes due to Potential Serious Eye Infection, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall - Flow Restrictor Bead May Become Displaced from its Fitting, FDA MedWatch
• Affordable Care Act at 3: Consumer Protections, Health Insurance Marketplace
• CVM Updates - FDA Gives Tips to Prevent Salmonella Infection from Handling Feeder Rodents and Pet Reptiles and Amphibians, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - An Overview of FDA's Public Meeting on Antiparasitic Drug Use and Resistance in Ruminants and Equines, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Med Prep Consulting Inc. Compounded Products: Recall - Potential Mold Contamination, FDA MedWatch
• Aumenta el robo de reembolsos de impuestos, GobiernoUSA.gov
• Update of CVM's What's New - Guidances Under Development for 2013, U.S. Food & Drug Administration (FDA)
• Vascular Solutions Zerusa Ltd. Issues Recall of Guardian II and Guardian II NC Hemostasis Valves, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Vascular Solutions Zerusa Ltd. Issues Recall of Guardian II and Guardian II NC Hemostasis Valves, U.S. Food & Drug Administration (FDA)
• Nishimoto Trading Co., LTD Issues Allergy Alert on Undeclared Milk in Kameda Brand 4.37 oz Packages of Rice Cracker "Kotsubukko", U.S. Food & Drug Administration (FDA)
• Grippo Foods Inc. Issues A Voluntary Recall Of All Sizes Of Their Plain Potato Chips, Bar-B-Q Potato Chips, Cheddar Cheese With A Touch Of Jalapeno Potato Chips, Hot Dill Pickle Potato Chips, Sweet Bermuda Onion Potato Chips And Salt & Vinegar Potato Chips Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of All Compounded Products Due To Potential Mold Contamination, U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of Magnesium Sulfate 2gm In Dextrose 5 percent In Water, 50ml For Injecton Due To Mold Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Stryker Instruments Neptune 1 Silver and Neptune 2 Ultra Waste Management System (Neptune 1 Silver and Neptune 2 Ultra): Safety Communication - Reports of Serious Tissue Damage and Patient Death, FDA MedWatch
• Hágase la prueba de detección del VIH, GobiernoUSA.gov
  • <Possible follow-ups>
  • Hágase la prueba de detección del VIH, GobiernoUSA.gov
  • Hágase la prueba de detección del VIH, GobiernoUSA.gov
• FDA MedWatch - Incretin Mimetic Drugs for Type 2 Diabetes: Early Communication - Reports of Possible Increased Risk of Pancreatitis and Pre-cancerous Findings of the Pancreas, FDA MedWatch
• ¿Conoce usted el sitio MedlinePlus en español?, GobiernoUSA.gov
• Update of CVM's What's New - Bravo! Recalls 2 lb Tubes of Chicken Blend-Raw Frozen Food Diet for Dogs and Cats (One Lot Code) Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Bravo! Recalls 2 lb Tubes of Chicken Blend-Raw Frozen Food Diet for Dogs and Cats (One Lot Code) Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 13, 2013, U.S. Food & Drug Administration (FDA)
• Nueva app de alerta de tornados, GobiernoUSA.gov
• New Breast Cancer Product Approval and Upcoming Workshop, FDA Office of Women's Health
• FDA approves Lymphoseek to help locate lymph nodes in patients with certain cancers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2013 Safety Labeling Changes includes 35 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - Azithromycin (Zithromax or Zmax): Drug Safety Communication - Risk of Potentially Fatal Heart Rhythms, FDA MedWatch
• Green Planet, Inc. Issues a Voluntary Nationwide Recall of One Lot of "Night Bullet," a Product Marketed as a Dietary Supplement to Support Male Sexual Performance, Due to Undeclared, Potentially Hazardous Active Ingredient, U.S. Food & Drug Administration (FDA)
• Premium Edge, Diamond Naturals and 4health Dry Cat Food Formulas Voluntarily Recalled Due to Possibility of Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Completes Work on Two Animal Drug User Fee Programs, U.S. Food & Drug Administration (FDA)
• The March 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• RECALL: Bumble Bee 5-Ounce Chunk White Albacore And Chunk Light Tuna, FoodSafety.gov
• RECALL:Chicken of the Sea 5-Ounce Chunk White Albacore Tuna in Water, FoodSafety.gov
• Update of CVM's What's New - Premium Edge, Diamond Naturals and 4health Dry Cat Food Formulas Voluntarily Recalled Due to Possibility of Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Diggin' Your Dog Recalls Strippin' Chicks Pet Treats Distributed in Colorado and Nevada Due to Possible Salmonella Hazard, U.S. Food & Drug Administration (FDA)
• Diggin’ Your Dog Recalls Strippin' Chicks Pet Treats Distributed in Colorado and Nevada Due to Possible Salmonella Hazard, U.S. Food & Drug Administration (FDA)
• Diggin’ Your Dog Recalls Strippin' Chicks Pet Treats Due to Possible Salmonella Hazard, U.S. Food & Drug Administration (FDA)
• Proteja sus derechos y no se deje engañar, 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 Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Cambio de hora este domingo, GobiernoUSA.gov
• Tri-union Seafoods Expands Recall To Include Chunk Light Tuna In Oil Products, U.S. Food & Drug Administration (FDA)
• Steve’s Real Food Recalls Turducken Canine Recipe Patties Because of Posssible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Steve’s Real Food Recalls Turducken Canine Recipe Patties Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Acoso escolar cómo identificarlo y eliminarlo, GobiernoUSA.gov
• FDA issues draft guidance for manufacturers to accurately label medical products that are not made with natural rubber latex, U.S. Food & Drug Administration (FDA)
• Bumble Bee Foods Expands Voluntary Recall on Specific Codes of 5-Ounce Chunk White Albacore and Chunk Light Tuna Products Due to Loose Seals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ad-Tech Macro Micro Subdural Electrodes Class 1 recall: Concern the microelectrodes are defective and may cause injury to the brain., FDA MedWatch
• Obtenga gratis una copia de la Guía del Consumidor, GobiernoUSA.gov
• Update of CVM's What's New - Small Entity Compliance Guide Available, U.S. Food & Drug Administration (FDA)
• Tri-Union Seafood Issues Voluntary Recall on Select 5-Ounce Chunk White Albacore Tuna in Water, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 06, 2013, U.S. Food & Drug Administration (FDA)
• Programas de asistencia alimentaria, GobiernoUSA.gov
• Bumble Bee Foods Issues Voluntary Recall On Specific Codes Of 5-Ounce Chunk White Albacore And Chunk Light Tuna Products Due To Loose Seals, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meetings with Food-Animal Producers and Veterinarians, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - ADUFA/AGDUFA Performance Reports, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CVM's New Animal Drugs for Use in Feeds Workshop, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cargill’s animal nutrition business conducts voluntary recall of select mineral product used in ruminant feed, U.S. Food & Drug Administration (FDA)
• Cargill’s animal nutrition business conducts voluntary recall of select mineral product used in ruminant feed, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Select Wheat Bread Products in Idaho, Oregon and Washington States, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - VICH Guidances Available, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: See’s Divinity Easter Egg with Walnuts (May Contain Peanut Butter), FoodSafety.gov
• RECALL: Pork Products by Seven Sons, Heffron Farms, and Byron Center Meats, FoodSafety.gov
• CVM Updates - FDA Seeks Comments on IFT Report on Product Tracing Pilots, U.S. Food & Drug Administration (FDA)
• See’s Candies, Inc. Issues Allergy Alert on 1.7oz Divinity Egg with Walnuts, code L.A.D. 102/13, U.S. Food & Drug Administration (FDA)
• Food For Life issues Recall - Allergy Alert - Undeclared Allergen in Food For Life Ezekiel 4:9 Cereal, U.S. Food & Drug Administration (FDA)
• Usted y la Semana Nacional de Protección del Consumidor, GobiernoUSA.gov
  • <Possible follow-ups>
  • Usted y la Semana Nacional de Protección del Consumidor, GobiernoUSA.gov
• Protéjase del fraude qué saber y qué hacer, GobiernoUSA.gov
• FDA Hepatitis Update - Vicrelis (boceprevir) label changes, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Prezista (darunavir) label change - drug interaction information, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Intelence (etravirine) labeling updates, U.S. Food & Drug Administration (FDA)
• Cómo hacer un plan de negocios, GobiernoUSA.gov
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience Reports, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals March 2013 Update, U.S. Food & Drug Administration (FDA)
• Ad-Tech Medical Instrument Corporation Issues Global Recall of Macro Micro Subdural Electrodes, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues International Food Safety Capacity-Building Plan under the Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - United Pet Group Inc. Recall, U.S. Food & Drug Administration (FDA)
• Zachary Confections, Inc. Announces Recall of Zachary Chocolate Covered Marshmallow Eggs due to Possible Contamination and Possible Health Risk, U.S. Food & Drug Administration (FDA)
• United Pet Group Inc., Voluntarily Withdraws "Ultra Blend Gourmet Food for Parakeets," "eCotrition Grains & Greens Nutritional Supplement for Parakeets," "eCotrition Grains & Greens Nutritional Supplement for Canaries and Finches," and "eCotrition Grains & Greens Nutritional Supplement for Cockatiels" Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 27, 2013, U.S. Food & Drug Administration (FDA)
• ¿Qué son los recortes automáticos?, GobiernoUSA.gov
• Cuide la salud del corazón con un examen cardiovascular, GobiernoUSA.gov
• Update of CVM's What's New - Letter to Kasel Associates Industries, Inc., U.S. Food & Drug Administration (FDA)
• Lion Pavilion Issues Alert on Undeclared Sulfites in Grassplot Ginger Slices, U.S. Food & Drug Administration (FDA)
• Domega NY International Co., Ltd Issues an Alert on Undeclared Sulfites in Green Day Brand White Melon Seeds, U.S. Food & Drug Administration (FDA)
• Teleconferencia de inmigración, GobiernoUSA.gov
• FDA MedWatch - Sensipar (Cinacalcet Hydrochloride): Drug Safety Communication - FDA Suspends Pediatric Clinical Trials After Report Of Death, FDA MedWatch
• FDA approves Osphena for postmenopausal women experiencing pain during sex, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves Drug to Assist with Cattle Breeding Regimens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lumenis VersaCut Tissue Morcellator: Class 1 Recall - Labeling Correction - Potential For Air Embolisms To Occur If Tubing Is Hooked Up Backwards, FDA MedWatch
• FDA approves Stivarga for advanced gastrointestinal stromal tumors, U.S. Food & Drug Administration (FDA)
• Olaax Corp. Issues a Nationwide Voluntary Recall of All Lots of Maxiloss Weight Advanced Softgels Dietary Supplement, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Hy-Vee Issues Voluntary Recall of Certain Dog Food Products, U.S. Food & Drug Administration (FDA)
• Herbalife Issues Allergy Alert due to Undeclared Milk Allergen in Instant Healthy Meal Nutritional Shake Mix Packets, U.S. Food & Drug Administration (FDA)
• King Arthur Flour Voluntarily Recalls Flour, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of Dakota Specialty Milling Select Flours and Grain Blends, U.S. Food & Drug Administration (FDA)
• Hy-Vee Issues VoluntaryRecall of Certain Dog Food Products, U.S. Food & Drug Administration (FDA)
• Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection, U.S. Food & Drug Administration (FDA)
• Bruce Foods Corporation Expands Recall to Indiana of Food Club Red Enchilada Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 20, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Omontys (peginesatide) Injection by Affymax and Takeda: Recall of All Lots - Serious Hypersensitivity Reactions, FDA MedWatch
• Bruce Foods Corporation Recall Food Club Red Enchilada Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Heartland Brands Voluntarily Recalls Two Varieties of Granola Cereals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - DePuy Orthopaedics LPS Diaphyseal Sleeve: Class I Recall - Taper Connection May Not Accommodate Physiologic Loads, FDA MedWatch
• FDA approves new treatment for late-stage breast cancer, U.S. Food & Drug Administration (FDA)
• Kaytee Recalls Bird Treats and Greens Due to Possible Salmonella Contamination from Parsley Flakes, U.S. Food & Drug Administration (FDA)
• Kasel Associates Industries Recalling Certain Pet Treats Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Undeclared Sulfites in Preserved Fruits, U.S. Food & Drug Administration (FDA)
• The Honest Kitchen® Voluntarily Recalls Limited Lots Of Verve®, Zeal®And Thrive® Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Goldcoast Salads Expands Voluntary Recall to Include Additional Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Mondelēz Global LLC Conducts Nationwide Voluntary Recall of belVita Breakfast Biscuit Apple Cinnamon and Chocolate Varieties in the U.S. and Puerto Rico, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Guidance for Industry #108 Available, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nutri-Vet, LLC Recalls Nutri-Vet and Nutripet Chicken Jerky Products Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Nutri-Vet, LLC Recalls Nutri-Vet and Nutripet Chicken Jerky Products Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Kasel Associated Industries Recalls All Products Manufactured at its Denver, Colorado Facility from April 20, 2012 thru September 19, 2012 Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves new silicone breast implant, U.S. Food & Drug Administration (FDA)
• Statement from Agriculture Secretary Tom Vilsack: World Organization for Animal Health Recommends United States' BSE Risk Status Be Upgraded, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kasel Associated Industries Recall, U.S. Food & Drug Administration (FDA)
• Voluntary Precautionary Recall Of Arnold, Brownberry, Earthgrains, Farm, Harmons, L’oven Fresh, Stroehmann and Sara Lee Multi-grain Breads and Sara Lee Thin Style Buns, U.S. Food & Drug Administration (FDA)
• Reumofan Plus USA, LLC and Reumofan USA, LLC is Voluntarily Recalling all lots of Reumofan Plus Tablets Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• MKG Provisions Voluntarily Recalls Atlantic Smoked Salmon Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nature's Variety Issues Voluntarily Recall of One Batch of Instinct® Raw Organic Chicken Formula for Dogs & Cats Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Caring for Someone with the Flu, Flu.gov
• Decoty Coffee Company Inc. Issues Allergy Alert On Undeclared Soy In Decoty Taco Seasoning, U.S. Food & Drug Administration (FDA)
• Nature's Variety Issues Voluntarily Recall of One Batch of Instinct® Raw Organic Chicken Formula for Dogs & Cats Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gilead Issues A Voluntary Recall Of One Lot Of Vistide® (CIDOFOVIR INJECTION) Due To Presence Of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vistide (Cidofovir Injection) by Gilead: Recall - Presence of Particulate Matter, FDA MedWatch
• Día de los Presidentes, GobiernoUSA.gov
• Pasos sencillos para crear un presupuesto, GobiernoUSA.gov
• What foods should pregnant women avoid? [Food Safe Fridays], FoodSafety.gov
• FDA Hepatitis Update - Victrelis (boceprevir) label updates, U.S. Food & Drug Administration (FDA)
• AMPI Issues Allergy Alert for Undeclared Milk in Pudding, U.S. Food & Drug Administration (FDA)
• JS Pelmini OK Inc Issues Allergy Alert On Undeclared Milk And Soy In Potato Dumplings And Potato And Mushroom Dumplings, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare, LLC, Giraffe and Panda T-Piece Resuscitation Systems and Mask Resuscitation Systems: Class 1 Recall - Potential Reversal of Oxygen/Air, FDA MedWatch
• U.S. Marshals seize drug products distributed by a Florida company, U.S. Food & Drug Administration (FDA)
• Domega NY International CO., LTD. Issues An Alert On Undeclared Sulfites In Green Day Brand Dried Coconut, U.S. Food & Drug Administration (FDA)
• ZIP International Group LLC Recalls Dry Salted Fish Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 13, 2013, U.S. Food & Drug Administration (FDA)
• Mantenga un corazón sano, GobiernoUSA.gov
  • <Possible follow-ups>
  • Mantenga un corazón sano, GobiernoUSA.gov
• FDA MedWatch - St. Jude Medical, AMPLATZER TorqVue FX Delivery System: Class I Recall - Core Wire May Fracture, FDA MedWatch
• Salinas Firm Initiates A Precautionary Recall Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Extends Comment Period on AquAdvantage Salmon Documents, U.S. Food & Drug Administration (FDA)
• The February 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• DZH Import & Export Inc. Issues an Alert on Undeclared Sulfites in Mountains Dried Mushroom, U.S. Food & Drug Administration (FDA)
• Pago electrónico de beneficios del Gobierno, GobiernoUSA.gov
• Ordene publicaciones gratis para mantener su corazón sano, GobiernoUSA.gov
• CVM Updates - FDA and JIFSAN Announce Online Training for Aquaculture Producers and Importers, U.S. Food & Drug Administration (FDA)
• Nestlé Prepared Foods Company Announces Voluntary Recall of LEAN CUISINE® Culinary Collection Mushroom Mezzaluna Ravioli, U.S. Food & Drug Administration (FDA)
• DZH Import & Export Inc. issues an alert on undeclared sulfites in Curiosity of Dashan Dried Mushroom, U.S. Food & Drug Administration (FDA)
• FDA approves Pomalyst for advanced multiple myeloma, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update _ Recent changes to the Reyataz (atazanavir sulfate) capsule labeling, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hamilton Medical, Inc., HAMILTON-T1 Ventilators with Software Versions 1.1.2 and Lower, FDA MedWatch
• UPDATED--Sprouters Northwest Expands Voluntary Recall to All Varieties of Sprouts Products, Wheatgrass, and Pea Shoots Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Muestre su cariño por el medio ambiente, GobiernoUSA.gov
• Update of CVM's What's New - 2013 Windows to Regulatory Research Internship Program, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals Monthly Update, U.S. Food & Drug Administration (FDA)
• FDA offers new guidance on developing drugs for Alzheimer’s disease, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Vet-LRN has changed its name to Vet-LIRN, U.S. Food & Drug Administration (FDA)
• GoldCoast Salads Voluntarily Recalls Blue Crab Spread Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 06, 2013, U.S. Food & Drug Administration (FDA)
• Salud dental en los niños, GobiernoUSA.gov
• Domega NY International Co., Ltd Issues an Alert on Undeclared Sulfites in Green Day Brand Dried Coconut, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Annual Report on Antimicrobials Sold or Distributed for Food-Producing Animals in 2011, U.S. Food & Drug Administration (FDA)
• Flu Risks for People with Heart Disease, Flu.gov
• FDA approval of generic version of cancer drug Doxil is expected to help resolve shortage, U.S. Food & Drug Administration (FDA)
• R-Kane Products, Inc. Issues Allergy Alert On Undeclared Soy And Milk In Z Pro High Protein Supplement, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Final Rule on Administrative Detention of Food, U.S. Food & Drug Administration (FDA)
• Tropical Nut and Fruit Co. Issues Allergy Alert on Undeclared Peanuts in “Chia Recharged Stix Mix” 5 Ounce Pouches, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Prepared Food Items Made with Circle Sea Salmon Lox Trim in Two States Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sprouter Northwest Expands Recall to All Varieties of Sprouts Products, Wheatgrass, and Pea Shoots with Any Best by Dates and All Sizes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lo esencial para la temporada de impuestos de 2013, GobiernoUSA.gov
• HIV/AIDS Update - Prezista (darunavir) tablet and oral suspension: pediatric dosing, U.S. Food & Drug Administration (FDA)
• Free Heart Health Kit for Women, FDA Office of Women's Health
• FDA approves new drug for the chronic management of some urea cycle disorders, U.S. Food & Drug Administration (FDA)
• What is the norovirus? [Food Safe Fridays], FoodSafety.gov
• Voluntary Field Correction Action Issued for GE Healthcare’s Resuscitation Systems with Blender Installed in GE Giraffe and Panda Infant Warmers, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 30, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vycor Viewsite Brain Access System (VBAS): Class 1 Recall - Unidentified Fiber Found on Device, FDA MedWatch
• Whole Foods Market Expands Its Recall Of Whole Catch Wild Alaskan Sockeye Salmon Because Of Possible Health Risk From Listeria, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Tyzeka (telbivudine) label revisions, U.S. Food & Drug Administration (FDA)
• Adults need vaccines too!, Vaccines.gov
• Sprouter Northwest Recalls Alfafa, Brocco Sandwich Sprouts, Clover, Spicy Sprouts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The Hartz Mountain Corporation is voluntarily withdrawing its Hartz Chicken Chews and Hartz Oinkies Pig Skin Twists wrapped with Chicken for dogs, U.S. Food & Drug Administration (FDA)
• Cómo reciclar en el invierno, GobiernoUSA.gov
• Update of CVM's What's New - Hartz Mountain Corporation Recall, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lactated Ringers and 5 Percent Dextrose Injection, USP, 1000 ML, Flexible Containers: Recall - Due to Non-Sterility, FDA MedWatch
• Freedom Trading Issues a Voluntary Nationwide Recall of Super Power, a Product Marketed as a Dietary Supplement to Support Male Sexual Performance, Due to Undeclared, Potentially Hazardous Active Ingredient, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Reorganization for the Foods and Veterinary Medicine Program, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recall Whole Catch Wild Alaskan Sockeye Salmon Because of Possible Health Risk from Listeria, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Labeling changes for Complera (emtricitabine/rilpivirine/tenofovir disoproxil fumarate), U.S. Food & Drug Administration (FDA)
• FDA approves three new drug treatments for type 2 diabetes, U.S. Food & Drug Administration (FDA)
• Proteja su computadora y sus datos de estafadores, GobiernoUSA.gov
• FDA approves Gleevec for children with acute lymphoblastic leukemia, U.S. Food & Drug Administration (FDA)
• First OTC Treatment for Overactive Bladder, FDA Office of Women's Health
• How do I safely prepare chicken? [Food Safe Fridays], FoodSafety.gov
• FDA approves over-the-counter Oxytrol for Women to treat overactive bladder, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Samsca (tolvaptan): Drug Warning - Potential Risk of Liver Injury, FDA MedWatch
• Enforcement Report for January 23, 2013, U.S. Food & Drug Administration (FDA)
• Specific Lots Of Hunt's Tomato Sauce Recalled For Can Defect, U.S. Food & Drug Administration (FDA)
• Winter eUpdate: New IUD, Safe Medication Use & More, FDA Office of Women's Health
• Voluntary Regional Recall Of Thomas', Sara Lee, Publix, And Weight Watchers Bagels, U.S. Food & Drug Administration (FDA)
• FDA approves Exjade to remove excess iron in patients with genetic blood disorder, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bausch and Lomb 27G Sterile Cannula Packed in Amvisc and Amvisc Plus Ophthalmic Viscosurgical Devices (OVD): Class I Recall - Cannulas May Leak or Detach From the Syringe, FDA MedWatch
• Flu Risks for Seniors, Flu.gov
• Annie's Voluntarily Recalls Annie's Homegrown Frozen Pizza Products, U.S. Food & Drug Administration (FDA)
• Sea un donante de sangre, GobiernoUSA.gov
• Evite estafas de inmigración, GobiernoUSA.gov
• HIV/AIDS Update - Kaletra (lopinavir/ritonavir) label update: drug interaction information, U.S. Food & Drug Administration (FDA)
• Knott's Fine Foods Recalls Chicken Salad Sandwiches Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 16, 2013, U.S. Food & Drug Administration (FDA)
• Día de Martin Luther King Jr., GobiernoUSA.gov
  • <Possible follow-ups>
  • Día de Martin Luther King Jr., GobiernoUSA.gov
• Cuatro años más de presidencia a partir del 20 de enero, GobiernoUSA.gov
• FDA MedWatch - Ferrous Sulfate Tablets, 325 mg Labeled as Rugby Natural Iron Supplement: Recall - Bottle May Contain Meclizine HCl 25 mg Tablets, FDA MedWatch
• When is my food thoroughly cooked? [Food Safe Fridays], FoodSafety.gov
• UPDATED - Allergy Alert – UNDECLARED EGGS in Kinnikinnick Foods Frozen Pie Crust, U.S. Food & Drug Administration (FDA)
• Advance Pharmaceutical Issues Nationwide Voluntary recall of one Lot (# 12G468) of Ferrous Sulfate Tablets, 325 mg, that may actually contain Meclizine HCl 25 mg tablets, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Webinar “ Draft Guidance Vaginal Microbicides: Development for the Prevention of HIV Infection", U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Metal-on-Metal Hip Implants: Safety Communication - Updated Safety Recommendations, FDA MedWatch
• FDA approves Octaplas to treat patients with blood clotting disorders, U.S. Food & Drug Administration (FDA)
• Treating the Flu, Flu.gov
• FDA approves new seasonal influenza vaccine made using novel technology, U.S. Food & Drug Administration (FDA)
• Edificios federales promueven la ecología y los espacios abiertos, GobiernoUSA.gov
• A new direction for HealthCare.gov, Health Insurance Marketplace
• Boba Direct Issues Allergy Alert on Undeclared Milk in BD Flavored Powders, U.S. Food & Drug Administration (FDA)
• Homestead Creamery Artisan Cheese Removed from Store Shelves, U.S. Food & Drug Administration (FDA)
• Belmont Confections Issues Allergy Alert on Undeclared Peanuts in "Dymatize Nutrition, Elite Gourmet Bars" (Cookies & Cream and Fudge Brownie), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - December 2012 Safety Labeling Changes includes 42 products with revisions to Prescribing Information, FDA MedWatch
• Lavarse las manos puede salvar vidas, GobiernoUSA.gov
• Update of CVM's What's New - Milo’s Kitchen® Voluntarily Recalls Chicken Jerky and Chicken Grillers Home-style Dog Treats, U.S. Food & Drug Administration (FDA)
• Milo’s Kitchen® Voluntarily Recalls Chicken Jerky and Chicken Grillers Home-style Dog Treats, U.S. Food & Drug Administration (FDA)
• Flu Season is Here--Take Action Now, Flu.gov
• Island Delights Volutarily Recalls Island Delights Coconut Haystack Candy Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• How do I safely cook with eggs? [Food Safe Fridays], FoodSafety.gov
• Enforcement Report for January 09, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mobius brand Mitosol (mitomycin for solution) Kit for Ophthalmic Use: Recall-May Not be Sterile, FDA MedWatch
• Update of CVM's What's New - FDA Announces Availability of the 2011 NARMS Retail Meat Annual Report, U.S. Food & Drug Administration (FDA)
• Giant & Martin's Alerts Customers To Voluntary Recall Of Ocean Beauty Seafood Smoked Salmon, U.S. Food & Drug Administration (FDA)
• The January 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA requires lower recommended doses for certain sleep drugs, FDA Office of Women's Health
• Mobius Therapeutics, LLC Issues a Voluntary Recall of Mitosol® (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use, U.S. Food & Drug Administration (FDA)
• Conozca cómo puede solicitar fondos del Gobierno para estudiar, GobiernoUSA.gov
• FDA MedWatch - Zolpidem Containing Products: Drug Safety Communication - FDA Requires Lower Recommended Doses, FDA MedWatch
• Update of CVM's What's New - 2012 ADUFA/AGDUFA Public Meeting Materials Available, U.S. Food & Drug Administration (FDA)
• Recall - Product Recall Because of Possible Listeria Monocytogenes Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Update on Jerky Treats, U.S. Food & Drug Administration (FDA)
• Seguro Social: nuevos servicios por Internet, GobiernoUSA.gov
• Conozca más sobre el glaucoma, GobiernoUSA.gov
• FDA issues draft guidance on abuse-deterrent opioids, U.S. Food & Drug Administration (FDA)
• Woodstock® Announces a Voluntary Recall for One Code Date of Mislabeled Woodstock Tamari Almonds Due to Undeclared Soy Allergen, U.S. Food & Drug Administration (FDA)
• Somersault Snack Co. Issues Allergy Alert on All Packages of Somersaults Cinnamon Crunch, U.S. Food & Drug Administration (FDA)
• Southwest Ice Cream Specialties Conducts Voluntary Recall of ShurFine® Brand “Creamery Select Premium Ice Cream Dulce de Leche” 1.75 Quarts Ice Cream Because Package May Contain Praline Pecan Ice Cream Which May Contain Undeclared Allergens (Wheat, Soy and Pecans), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fisher and Paykel Healthcare Reusable Breathing Circuit: Class I Recall - Pinholes in Tubes, FDA MedWatch
• Update of CVM's What's New - January 2013 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• ANDY CAPP’S HOT FRIES RECALLED DUE TO UNDECLARED SOY ALLERGEN, U.S. Food & Drug Administration (FDA)
• Prevención del cáncer en las mujeres, GobiernoUSA.gov
• Are raw sprouts safe to eat? [Food Safe Fridays], FoodSafety.gov
• FDA proposes new food safety standards for foodborne illness prevention and produce safety, U.S. Food & Drug Administration (FDA)
• Gilster-Mary Lee Corp. Issues Allergy Alert on Undeclared Tree Nuts in Food Club Chocolate Chunk Brownie Mix., U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 02, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Praxair Inc., Grab ‘n Go Vantage Portable Oxygen Cylinder Units: Class I Recall - Risk of Fire Inside Cylinder Unit, FDA MedWatch
• Allergy Alert – Undeclared Eggs in Kinnikinnick Foods Frozen Pie Crust, U.S. Food & Drug Administration (FDA)
• Cómo escoger una agencia de asesoría de crédito, GobiernoUSA.gov
• HIV/AIDS Update - Approval of Fulyzaq (crofelemer) to relieve symptoms of diarrhea in HIV/AIDS patients taking antiretroviral therapy, U.S. Food & Drug Administration (FDA)
• ¡Feliz 2013!, GobiernoUSA.gov
• Looking Forward to 2013, HealthCare.gov
• Despídase del 2012 de manera segura, GobiernoUSA.gov
• FDA approves first anti-diarrheal drug for HIV/AIDS patients, U.S. Food & Drug Administration (FDA)
• Procesadora de Productos Marinos Delifish S.A. Recalls Product Because Of Possible Listeria Monocytogenes Risk, U.S. Food & Drug Administration (FDA)
• FDA approves first drug to treat multi-drug resistant tuberculosis, U.S. Food & Drug Administration (FDA)
• Urgent: ADM Alliance Nutrition Recalling MoorMan’s® ShowTec® 18 Elite Lamb Feed, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 26, 2012, U.S. Food & Drug Administration (FDA)
• Si va al volante, vaya sobrio, GobiernoUSA.gov
• Resoluciones de Año Nuevo: cúmplalas, GobiernoUSA.gov
• FDA MedWatch - GE Healthcare T-Piece Circuits for the Giraffe and Panda Resuscitation Systems: Class I Recall – Failure to Achieve the Desired Inspiratory Pressure During Ventilation, FDA MedWatch
• What should I know about food poisoning? [Food Safe Fridays], FoodSafety.gov
• FDA MedWatch - Zimmer Spine - PEEK Ardis Inserter: Class I Recall – Risk of Implant Breakage, FDA MedWatch
• Voluntary Worldwide Field Corrective Action Issued for the T-piece Circuit used on GE Healthcare’s Giraffe and Panda, U.S. Food & Drug Administration (FDA)
• It’s Not Too Late to Vaccinate!, Flu.gov
• Haig’s Delicacies Announces Voluntary Recall of Tzatziki, Falafel, Spanakopita and, U.S. Food & Drug Administration (FDA)
• Ajuste del costo de vida en 2013, GobiernoUSA.gov
• FDA approves new orphan drug for rare cholesterol disorder, U.S. Food & Drug Administration (FDA)
• ¡Feliz Navidad!, GobiernoUSA.gov
• FDA MedWatch - Ventlab Adult and Pediatric Manual Resuscitators: Recall-Valve Leak Prevents Flow of Air/Oxygen to Patient, FDA MedWatch
• FDA MedWatch - Bunnell Life Pulse High-Frequency Ventilator Patient Circuits: Recall- Melted Insulation Can Cause Sparking and Smoke, FDA MedWatch
• FDA MedWatch - Medtronic Drug Infusion Pumps: Recall - Intermittent or Permanent Pump Motor Stall, FDA MedWatch
• FDA MedWatch - Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg: Recall - Potential for Oversized Tablets, FDA MedWatch
• FDA Hepatitis Update - Important safety information and labeling changes for Incivek (telaprevir), U.S. Food & Drug Administration (FDA)
• S&M INTERNATIONAL INC. Recalls Yang Sheng Cooked Salted Duck Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Praxair, Inc. has Initiated a Voluntary Recall Affecting Grab ‘n Go®Vantage Portable Oxygen Cylinder Units, U.S. Food & Drug Administration (FDA)
• FDA expands Tamiflu’s use to treat children younger than 1 year, U.S. Food & Drug Administration (FDA)
• P&J Trading Issues a Voluntary Recall of All Lots of the Dietary Supplements Slimdia Revolution, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - AquAdvantage Salmon Environmental Assessment Available, U.S. Food & Drug Administration (FDA)
• FDA approves Gattex to treat short bowel syndrome, U.S. Food & Drug Administration (FDA)
• Voluntary Product Recall Initiated by Qualitest Pharmaceuticals Impacts Three Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Repackaged and Distributed by Mylan Institutional, U.S. Food & Drug Administration (FDA)
• Could it be Salmonella? [Food Safe Fridays], FoodSafety.gov
• Food Safe Fridays are (almost) here!, FoodSafety.gov
• Invacare signs consent decree to correct wheelchair manufacturing problems, U.S. Food & Drug Administration (FDA)
• Zimmer Spine Issues Urgent Worldwide Medical Device Recall Of The Inserter Instrument For The PEEK Ardis Interbody Spacer, U.S. Food & Drug Administration (FDA)
• True Taste, LLC Recalls, "Hot Smoked Rainbow Trout, Hot Smoked Whitefish, Hot Smoked Herring, Hot Smoked Mackerel, Hot Smoked Salmon Steak, Cold Smoked Mackerel, And Cold Smoked Whitefish" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Aplicaciones móviles del Gobierno, GobiernoUSA.gov
• Are You a Physician on the Move? New Mobile App Keeps You Connected this Flu Season!, Flu.gov
• Udi’s Healthy Foods, LLC Issues Allergy Alert for Undeclared Almonds in 12-ounce "Udi’s Gluten Free Au Naturel Granola", U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 19, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Pradaxa (dabigatran etexilate mesylate): Drug Safety Communication - Should Not Be Used in Patients with Mechanical Prosthetic Heart Valves, FDA MedWatch
• Prepárese para el invierno, GobiernoUSA.gov
• FDA MedWatch - Incivek (telaprevir) In Combination with Drugs Peginterferon Alfa and Ribavirin (Incivek combination treatment): Drug Safety Communication - Serious Skin Reactions, FDA MedWatch
• Publicaciones gratis para empezar bien el año, GobiernoUSA.gov
• Resuelva tomar menos durante las fiestas, GobiernoUSA.gov
• FDA MedWatch - Zicam Extreme Congestion Relief Nasal Gel: Recall - Contamination With Burkholderia Cepacia, FDA MedWatch
• True Taste, LLC RECALLS, "Hot Smoked Rainbow Trout, Hot Smoked Whitefish, Hot Smoked Herring, Hot Smoked Mackerel, Hot Smoked Salmon Steak, Cold Smoked Mackerel, and Cold Smoked Whitefish", U.S. Food & Drug Administration (FDA)
• Matrixx Initiatives Issues Nationwide Voluntary Recall of One Lot of Zicam®, U.S. Food & Drug Administration (FDA)
• Recall – Performance Plus Marketing Press Release, U.S. Food & Drug Administration (FDA)
• States Are Moving Forward, HealthCare.gov
• Modifican medidas de seguridad en los aeropuertos, GobiernoUSA.gov
• Cocine con cariño y precaución, GobiernoUSA.gov
• FDA MedWatch - Xyrem (sodium oxybate): Drug Safety Communication - Warning Against Use With Alcohol or Drugs Causing Respiratory Depression, FDA MedWatch
• Hospira Issues Voluntary Nationwide Recall of Three Lots of Carboplatin Injection Due to Visible Particulate Matter, U.S. Food & Drug Administration (FDA)
• Ocean Beauty Seafoods LLC Recalls “Nathan’s Brand Cold Smoked Atlantic Salmon 3 oz” and “LASCCO Cold Smoked Atlantic Salmon 4 oz”, U.S. Food & Drug Administration (FDA)
• Extienda la mano a los que sufren de depresión durante las fiestas, GobiernoUSA.gov
• FDA MedWatch - Carboplatin Injection by Hospira: Recall - Visible Particulate Matter Identified, FDA MedWatch
• FDA approves raxibacumab to treat inhalational anthrax, U.S. Food & Drug Administration (FDA)
• FDA approves Iclusig to treat two rare types of leukemia, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ethicon, Inc., SURGIFLO Hemostatic Matrix and SURGIFLO Hemostatic Matrix Kit Plus FlexTip with Thrombin: Class I Recall - Potential for Packaging Breach, FDA MedWatch
• FDA MedWatch - Verathon GlideScope Video Laryngoscope Reusable Blades: Class 1 Recall - Breaking Across the Tip of the Blade, FDA MedWatch
• Salinas Firm Conducts Precautionary Recall On A Select Salad Product Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Claudia’s Canine Cuisine® Voluntarily Recalls it’s Dogcandy® Brand of Holiday Hound Cake and Blueberry Hound Cake, U.S. Food & Drug Administration (FDA)
• Claudia’s Canine Cuisine® Voluntarily Recalls it’s Dogcandy® Brand of Holiday Hound Cake (7.5 Oz.) and Blueberry Hound Cake (7.5 Oz) Manufactured for, Distributed, and Sold in Approximately 130 Petsmart Stores Because of The Possibility of Mold, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 12, 2012, U.S. Food & Drug Administration (FDA)
• Season's Greetings from FDA Office of Women's Health, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chantix (Varenicline): Safety Communication - Updated Safety Review On The Risk of Cardiovascular Adverse Events, FDA MedWatch
• CVM Updates - FDA and Health Canada announce first simultaneous review and approval of a veterinary drug product, U.S. Food & Drug Administration (FDA)
• Toma de posesión presidencial y eventos inaugurales, GobiernoUSA.gov
• FDA MedWatch - Natus Medical Incorporated, Olympic Cool-Cap System: Class I Recall - Control Screen Freezes During Treatment, FDA MedWatch
• Discapacidades y calidad de vida, en GobiernoUSA.gov, GobiernoUSA.gov
• Stay Flu-Free This Holiday Season, Flu.gov
• Mister Snacks, Inc. Issues Allergy Alert on Undeclared Peanuts in 5oz. Packages of Yogurt Raisins, U.S. Food & Drug Administration (FDA)
• Freshway Foods Voluntarily Recalls Out-of-Date Sliced Apples Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Decore su casa a prueba de incendios, GobiernoUSA.gov
• HIV/AIDS Update - Labeling updates for Edurant (rilpivirine), U.S. Food & Drug Administration (FDA)
• Progress Continues in Setting Up Health Insurance Marketplaces, HealthCare.gov
• FDA expands Zytiga’s use for late-stage prostate cancer, U.S. Food & Drug Administration (FDA)
• Upcoming FDA Meetings, U.S. Food & Drug Administration (FDA)
• Sugar Flowers Plus Inc Issues Allergy Alert on Undeclared Egg White in Cake Decors Pastillage (gumpaste) Flowers, U.S. Food & Drug Administration (FDA)
• Recall (Worchester, MA): Price Chopper Supermarkets Pumpkin & Cinnamon Coffee Cakes, FoodSafety.gov
• Recall: Free Bird Fully Cooked Breaded Chicken Products, FoodSafety.gov
• FDA MedWatch - Protandim by LifeVantage Corporation: Recall - Possible Metal Fragments in Product, FDA MedWatch
• LifeVantage Corporation Announces Voluntary Recall and Replacement of Select Lots of Protandim® Dietary Supplement Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Qualitest Issues Voluntary, Nationwide Recall of 101 Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, Usp 10 Mg/500 Mg Due to the Potential for Oversized Tablets, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heparin: Drug Safety Communication - Important change to heparin container labels to clearly state the total drug strength, FDA MedWatch
• CVM Updates - FDA: Don’t feed certain Nature’s Deli Chicken Jerky Dog treats, U.S. Food & Drug Administration (FDA)
• Who's at Risk for the Flu?, Flu.gov
• Enforcement Report for December 05, 2012, U.S. Food & Drug Administration (FDA)
• Bunnell Incorporated Issues Nationwide Recall Notification of Life Pulse High-Frequency Ventilator Patient Circuits, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces 2012 Public Meetings and Comment Periods for Reauthorization of ADUFA and AGDUFA Programs, U.S. Food & Drug Administration (FDA)
• Recall: Cantina Foods Beef and Cheese Pastellios, FoodSafety.gov
• Update of CVM's What's New - Proposed Rule; New Animal Drugs; Updating Tolerances for Residues of New Animal Drugs in Food, U.S. Food & Drug Administration (FDA)
• Stop & Shop alerts customers to voluntary recall of, U.S. Food & Drug Administration (FDA)
• Price Chopper Supermarkets Recalls Central Market Classic Cinnamon Coffee Cake Purchased At Mountain Road Store In Worcester, MA, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ondansetron (Zofran) 32 mg, Single Intravenous (IV) Dose: Updated Safety Communication – Product Removal due to Potential For Serious Cardiac Risks, FDA MedWatch
• Update of CVM's What's New - December 2012 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• It's Not Too Late! Open Enrollment Ends December 7, HealthCare.gov
• ¿Ya se vacunó contra la gripe?, GobiernoUSA.gov
  • <Possible follow-ups>
  • ¿Ya se vacunó contra la gripe?, GobiernoUSA.gov
• 10 consejos para las fiestas, GobiernoUSA.gov
  • <Possible follow-ups>
  • 10 consejos para las fiestas, GobiernoUSA.gov
• Recall: Aliya's Butter Chicken With Basmati Rice frozen meals, FoodSafety.gov
• Recall: Veggie Patch Ultimate Meatless Burger and Veggie Patch Falafel, FoodSafety.gov
• FDA announces public-private partnership to develop regulatory science that will speed patient access to new medical device technologies, U.S. Food & Drug Administration (FDA)
• Flu Prevention and Vaccination, Flu.gov
• Verathon Inc. Issues Voluntary Recall of Certain GlideScope GVL Video Laryngoscope Reusable Blades, U.S. Food & Drug Administration (FDA)
• VEGGIE PATCH Voluntarily Recalls Two Items- The Ultimate Meatless Burger and Falafel- Due To Possible Risk Of Contamination By Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - December 1 - World AIDS Day, U.S. Food & Drug Administration (FDA)
• Flu Risks for People Living with HIV, Flu.gov
• Participe en un "enlace" sobre temas migratorios, GobiernoUSA.gov
• Hay que mantenerse saludable y activo durante las fiestas, GobiernoUSA.gov
• FDA MedWatch - Mindray A3 and A5 Anesthesia Delivery System: Class I Recall - Gasket Leak, FDA MedWatch
• FDA Hepatitis Update - Hepsera (adefovir dipivoxil) package insert updated to add new safety information, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Hepsera (adefovir dipivoxil) package insert updated to add new safety information, U.S. Food & Drug Administration (FDA)
• FDA approves Cometriq to treat rare type of thyroid cancer, U.S. Food & Drug Administration (FDA)
• The December 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Allergy Alert: Sukhi's Gourmet Indian Red Curry Vegetables, FoodSafety.gov
• Sukhi's Gourmet Indian Foods issues voluntary recall of Sukhi's Red Curry Vegetables due to undeclared Shrimp, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 28, 2012, U.S. Food & Drug Administration (FDA)
• Bracco Diagnostics Inc. Issues Voluntary Nationwide Recall of Isovue® (iopamidol injection) Pre-Filled Power Injector Syringes due to Presence of Particulates, U.S. Food & Drug Administration (FDA)
• Ranbaxy Issues Voluntary Nationwide Recall Of 41 Lots Of Atorvastatin Calcium Tablets 10 Mg, 20 Mg And 40 Mg Due To Potential Presence Of Foreign Substance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Atorvastatin Calcium Tablets by Ranbaxy Inc.: Recall - Presence of Foreign Substance, FDA MedWatch
• FDA MedWatch - Isovue (iopamidol injection) Pre-Filled Power Injector Syringes by Bracco Diagnostics Inc.: Recall - Presence of Particulates, FDA MedWatch
• Update of CVM's What's New - Notice of Public Meeting; Framework for Pharmacy Compounding; State and Federal Roles, U.S. Food & Drug Administration (FDA)
• Allergy Alert: Newman’s Own Lite Honey Mustard - Undeclared Milk, FoodSafety.gov
• Recall: Capital City Fruit - Cherry Tomatoes, FoodSafety.gov
• Update of CVM's What's New - FDA Suspends Sunland Inc.'s Food Facility Registration, U.S. Food & Drug Administration (FDA)
• Capital City Fruit Issues Voluntary Recall on Cherry Tomatoes Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update- Draft guidance on vaginal microbicides for the prevention of HIV infection, U.S. Food & Drug Administration (FDA)
• Newman’s Own, Inc. Issues Voluntary Recall of Newman’s Own Lite Honey Mustard Dressing Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Newman’s Own, Inc. Issues Voluntary Recall of Newman’s Own Lite Honey Mustard Dressing Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Issues Allergy Alert on Undeclared, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Carolina Prime Pet Inc. Announces Recall Of Priority Total Pet Care All Natural Bullstrips, U.S. Food & Drug Administration (FDA)
• Voluntary Precautionary Product Recall, U.S. Food & Drug Administration (FDA)
• Rio Queen Citrus, Inc. Recalls Cherry Tomatoes Because Of Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 21, 2012, U.S. Food & Drug Administration (FDA)
• Disfrute de las fiestas con comida deliciosa e inocua, GobiernoUSA.gov
• Drug Shortages Update 11/20/2012, U.S. Food & Drug Administration (FDA)
• Carolina Prime Pet Inc. Announces Recall Of Priority Total Pet Care All Natural Bullstrips Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Recall: Michael Gourmet Wild Alaskan Sockeye Salmon (Whole Foods Markets - FL), FoodSafety.gov
• Whole Foods Market Recalls Cookies Due to Undeclared Nut Allergens, U.S. Food & Drug Administration (FDA)
• Whole Alternatives, LLC Recalls Harris Teeter Dried Apricots and Dried Golden, U.S. Food & Drug Administration (FDA)
• Boulder Ice Cream Announces a Voluntary Limited Recall of Ice Cream and Gelato Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Michaels Gourmet Delicacies, U.S. Food & Drug Administration (FDA)
• ¡Feliz Día de Acción de Gracias!, GobiernoUSA.gov
  • <Possible follow-ups>
  • ¡Feliz Día de Acción de Gracias!, GobiernoUSA.gov
• Moving Forward, HealthCare.gov
• Drug Shortages Update 11/19/2012, U.S. Food & Drug Administration (FDA)
• Nationwide Recall: Cocoa Latte™ Hot Drink Maker Due to Lead Risk, FoodSafety.gov
• Viaje seguro, tranquilo y sin prisas, GobiernoUSA.gov
• Obtenga su declaración del Seguro Social, GobiernoUSA.gov
• FDA MedWatch - HeartSine Samaritan Public Access Defibrillator 300/300P: Class I Recall - Device May Intermittently Turn On and Off, FDA MedWatch
• Update of CVM's What's New - New Guidance Available, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Magnolia Bird Farm, Inc. Recalls Peanuts and Seed Mixes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Focus Products Group International, LLC Announces a Nationwide Recall of Cocoa Latte™ Hot Drink Makers Due to Possible Lead Risk, U.S. Food & Drug Administration (FDA)
• Tony’s Import and Exports warns of Tahineh (Sesame Paste), U.S. Food & Drug Administration (FDA)
• Tri-union Seafoods Issues Voluntary Recall On Select 7-ounce Solid White Albacore Tuna In Water, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 14, 2012, U.S. Food & Drug Administration (FDA)
• Magnolia Bird Farm, Inc. Recalls Peanuts and Seed Mixes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Updated - Berres Brothers Coffee Roasters Issues Allergy Alert On Possible Nut Flavoring In Coffee, U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall Multiple Cake Products, U.S. Food & Drug Administration (FDA)
• Consejos para hacer compras seguras por Internet, GobiernoUSA.gov
• Is it a cold or the flu?, Flu.gov
• ¿Por qué vale la pena reciclar?, GobiernoUSA.gov
• Prevention & Wellness: Be Tobacco Free, HealthCare.gov
• Diabetes: cómo controlarla, GobiernoUSA.gov
  • <Possible follow-ups>
  • Diabetes: cómo controlarla, GobiernoUSA.gov
• Turkana Food Inc. Recalls “Turkana Valley” Brand Dried Apricots Due to the Presence of Undeclared Sulfites, U.S. Food & Drug Administration (FDA)
• Recursos para cuidadores de pacientes con enfermedad de Alzheimer, GobiernoUSA.gov
  • <Possible follow-ups>
  • Recursos para cuidadores de pacientes con enfermedad de Alzheimer, GobiernoUSA.gov
• FDA MedWatch - October 2012 Safety Labeling Changes includes 58 products with revisions to Prescribing Information, FDA MedWatch
• Kenny's Farmhouse Cheese Issues a Voluntary Recall of Various Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Viramune XR (nevirapine) label includes new 100 mg tablet and added dosing information, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Prezista (darunavir) availability of 800 mg tablet strength, U.S. Food & Drug Administration (FDA)
• Mindray DS USA, Inc. has initiated a voluntary recall affecting the A3/A5 Anesthesia Delivery System, U.S. Food & Drug Administration (FDA)
• Uso adecuado de antibióticos, GobiernoUSA.gov
  • <Possible follow-ups>
  • Uso adecuado de antibióticos, GobiernoUSA.gov
  • Uso adecuado de antibióticos, GobiernoUSA.gov
• Recall: Bourbon Barbecue Sausage by Pinnacle Foods, FoodSafety.gov
• Alergy Alert: Grandma's Peanut Butter Sandwich Creme Cookies, FoodSafety.gov
• Allergy Alert: Jimmy Dean French Toast & Sausage Sandwich, FoodSafety.gov
• Jimmy Dean® French Toast & Sausage Sandwich for Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Spence and Co Issues A Voluntary Recall of 4oz New York Style Nova Lox Lot Number 9720704 Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Frito-Lay Issues Voluntary Recall of GRANDMA'S Peanut Butter Sandwich Creme Cookies and GRANDMA's Peanut Butter Mini Sandwich Creme Cookies Due to Undeclared Milk and Egg, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval fixed dose efavirenz, lamivudine and tenofovir disoproxil fumarate fixed-dose tablets, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - tentative approval fixed dose lamivudine and tenofovir disoproxil fumarate, U.S. Food & Drug Administration (FDA)
• Alert: Undeclared Sulfites In Fu Xiang Yuan "Lily Dry", FoodSafety.gov
• Recall: Fresh Express 9 oz. Spinach, FoodSafety.gov
• Recall: NESQUIK' Chocolate Powder, FoodSafety.gov
• Nestlé USA Announces Voluntary Recall of NESQUIK® Chocolate Powder, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 07, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baxter Healthcare Corp. Buretrol Solution Set: Class 1 Recall - May Not Function as Expected, FDA MedWatch
• Fresh Express Recalls Limited Quantity of 9 oz. Spinach Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Consumer Alert - Undeclared Sulfites In Fu Xiang Yuan Trading Inc "Lily Dry", U.S. Food & Drug Administration (FDA)
• Please help provide feedback on the FDA’s Food website, FoodSafety.gov
  • <Possible follow-ups>
  • Please help provide feedback on the FDA’s Food website, U.S. Food & Drug Administration (FDA)
• Recall: Bolthouse Farms Carrot Chips (16 oz), FoodSafety.gov
• Allergy Alert: Perdue Chicken Breast Nuggets - Undeclared Milk Allergen, FoodSafety.gov
• Update of CVM's What's New - Medication Errors Happen to Pets, Too, U.S. Food & Drug Administration (FDA)
• Omya Voluntarily Recalls Ground Limestone Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Xeljanz for rheumatoid arthritis, U.S. Food & Drug Administration (FDA)
• Select Containers of Kroger Deluxe French Vanilla Ice Cream, U.S. Food & Drug Administration (FDA)
• 10 formas de ahorrar energía en el invierno, GobiernoUSA.gov
  • <Possible follow-ups>
  • 10 formas de ahorrar energía en el invierno, GobiernoUSA.gov
• Wegmans Pumpkin Roll is Recalled Because the Product May Contain Pieces of Plastic, U.S. Food & Drug Administration (FDA)
• The Raymond-Hadley Corporation Expands Voluntary Recall to Include Additional Enjoy by Dates on Webmans Gluten Free Mixes Including: Double Chocolate Brownie Mix 17.2 oz., All Purpose Baking Mix 16oz., Honey Cornbread Mix 16oz., and Chocolate Cake Mix 15.3oz., U.S. Food & Drug Administration (FDA)
• Amended Bolthouse Farms Voluntarily Recalls Limited Quantity Of 16-Ounce Carrot Chips, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets, Inc. Announces Recall of 5 oz. and 11 oz. Organic Spinach & Spring Mix Blend - May be Contaminated with E.coli O157 H:7, U.S. Food & Drug Administration (FDA)
• Faltan pocos días para votar: esté listo, GobiernoUSA.gov
• Huracán Sandy: recuperación y respuesta, GobiernoUSA.gov
• FDA expands use of Xarelto to treat, reduce recurrence of blood clots, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Victrelis (boceprevir) labeling update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Charlee Bear Products Recalls “Protein Crunch Bars” Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• The November 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Charlee Bear Products Recalls “Protein Crunch Bars” Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Bolthouse Farms Voluntarily Recalls Limited Quantity Of 16-Ounce Carrot Chips, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 31, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Laboratory Results from Samples of Additional NECC Products Tested Positive For Bacterial Contamination, FDA MedWatch
• Cómo prepararse para una cita médica, GobiernoUSA.gov
• ¿Está listo para votar el 6 de noviembre?, GobiernoUSA.gov
• Update of CVM's What's New - November 2012 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Wegmans Recalls Gluten Free Baking Products - Chocolate Cake Mix, Food You Feel Good About Gluten Free Honey Cornbread Mix, and Food You Feel Good About All Purpose Baking Mix Because Products May Contain Undeclared Soy, U.S. Food & Drug Administration (FDA)
• Flu Risks for People with Diabetes, Flu.gov
• FDA MedWatch - Ameridose, LLC: Recall of Unexpired Products in Circulation, FDA MedWatch
• Recall: Bremer Frozen Chicken Enchiladas, FoodSafety.gov
• Allergy Alert: Tropical Valley Foods Bulk Dark Chocolate, Milk Chocolate and Trail Mix Products, FoodSafety.gov
• Recall: ZuPreem Bird Foods due to Health Risk, FoodSafety.gov
• Ameridose Issues Recall of All Products, U.S. Food & Drug Administration (FDA)
• Zi Xiu Tang Success, LLC Issues Voluntary Nationwide Recall Of Classic Zi Xiu Tang Bee Pollen Capsules And Ultimate Formula Capsules Due To Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Recuperación de los efectos de Sandy, GobiernoUSA.gov
• Hospira Issues A Voluntary Nationwide Recall Of Symbiq Infusion Systems Due To Inaccurate Response Of The Touch Screen To User Selection/Input, U.S. Food & Drug Administration (FDA)
• BT McElrath Chocolatier, Inc. Announces Nationwide Recall Of Peanut Butter Pave Due To Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Schoep's Ice Cream Company Issues Allergy Alert On Undeclared Allergen In Kays Classic Vanilla Bean Ice Cream, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Symbiq Infusion System Touchscreen: Class 1 Recall - May Not Respond to Selection, FDA MedWatch
• Update of CVM's What's New - Premium Nutritional Products Announces Ongoing Voluntary Recall Of Select ZuPreem Bird Foods, U.S. Food & Drug Administration (FDA)
• Premium Nutritional Products Announces Ongoing Voluntary Recall Of Select ZuPreem Bird Foods, U.S. Food & Drug Administration (FDA)
• FDA reports conditions observed at New England Compounding Center facility, U.S. Food & Drug Administration (FDA)
• Huracán Sandy: esté preparado, GobiernoUSA.gov
• FDA MedWatch - Ethicon Endo-Surgery Circular Stapler Sets: Class I Recall - User Difficulty With Firing Stapler Devices, FDA MedWatch
• FDA MedWatch - Stryker Neptune Rover Waste Management Systems (UPDATE) - Class I Recall, FDA MedWatch
• FDA approves Synribo for chronic myelogenous leukemia, U.S. Food & Drug Administration (FDA)
• Bumble Bar, Inc. Recalls Gluten Free Cafe™ Chocolate Sesame Bars and Gluten Free Cafe™ Cinnamon Sesame Bars Due to Possible Health Risk Associated With Sunland Inc. Peanut Products, U.S. Food & Drug Administration (FDA)
• Tropical Valley Foods Issues Alert On Undeclared Allergens In Dark Chocolate, Organic Dark Chocolate, Milk Chocolate And Trail Mix Products Sold In Bulk, U.S. Food & Drug Administration (FDA)
• HeartSine Technologies, Ltd. Issues Global Correction Of Samaritan® 300/300P PAD, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • HeartSine Technologies, Ltd. Issues Global Correction of Samaritan® 300/300P PAD, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Over-The-Counter Eye Drops and Nasal Sprays: Drug Safety Communication - Serious Adverse Events From Accidental Ingestion by Children, FDA MedWatch