FDA News Releases

• Date Index

• FDA MedWatch - Nitroglycerin in 5% Dextrose Injection by Baxter: Recall - Particulate Matter, FDA MedWatch
• Baxter Initiates Nationwide Voluntary Recall of One Lot of Nitroglycerin in 5% Dextrose Injection, U.S. Food & Drug Administration (FDA)
• Zip International Group LLC Recalls Herring Fillet in Oil Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA study helps provide an understanding of rising rates of whooping cough and response to vaccination, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Spacelabs Healthcare, Inc., Spacelabs Anesthesia Workstations and Service Kits, U.S. Food & Drug Administration (FDA)
• Proteja su información al comprar por Internet, GobiernoUSA.gov
• FDA MedWatch - Spacelabs Healthcare, Inc., Spacelabs Anesthesia Workstations and Service Kits: Class I Recall - Bag-to-Vent Switch in CAS I/II Absorbers May Fail, FDA MedWatch
• FDA MedWatch - CLR Medicals International Inc. Viscoelastic Products: Recall - Quality System Deficiencies And Lack Of Premarket Approval (PMR), FDA MedWatch
• CLR Medicals International Inc. Issues Nationwide Recall of Viscoelastic Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira GemStar Infusion System: Class I Recall - Pressure Sensor Calibration Drift, FDA MedWatch
• FDA requires removal of certain restrictions on the diabetes drug Avandia, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Rosiglitazone-containing Diabetes Medicines: Drug Safety Communication - Removal of Some Prescribing and Dispensing Restrictions, FDA MedWatch
• Medical Device Safety and Recalls: Hospira Inc., GemStar Infusion System - Pressure Sensor Calibration Drift, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Olysio (simeprevir) for the treatment of chronic hepatitis C in combination antiviral treatment, U.S. Food & Drug Administration (FDA)
• Jayone Food Issues Voluntary Alert on Undeclared Peanuts in Dried Seaweed Salad, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 20, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Meridian Medical Technologies Auto-Injectors: Extension of Expiration Dates, FDA MedWatch
• FDA approves Nexavar to treat type of thyroid cancer, U.S. Food & Drug Administration (FDA)
• FDA approves first adjuvanted vaccine for prevention of H5N1 avian influenza, U.S. Food & Drug Administration (FDA)
• Gasolina: encuentre los mejores precios, GobiernoUSA.gov
• Update of CVM's What's New - Veterinary Medicine Advisory Committee Disbands, U.S. Food & Drug Administration (FDA)
• Check medicines to avoid taking too much acetaminophen this cold and flu season, U.S. Food & Drug Administration (FDA)
• Deseo Rebajar Inc. Issues Voluntary Puerto Rico Recall of Adipotrim XT Due to Underclared Fluoxetine, U.S. Food & Drug Administration (FDA)
• Marina's German Bakery Issues Allergy Alert on Undeclared Almonds, Walnuts, and Hazelnuts in Pastry Products, U.S. Food & Drug Administration (FDA)
• Día Nacional de No Fumar, GobiernoUSA.gov
• FDA MedWatch - Lexiscan (regadenoson) and Adenoscan (adenosine): Drug Safety Communication - Rare but Serious Risk of Heart Attack and Death, FDA MedWatch
• Tendex Issues Voluntary Nationwide Recall of P-Boost, NatuRECT Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Public Meeting Agendas Available, U.S. Food & Drug Administration (FDA)
• Blount Fine Foods Voluntary Recall of “Wegmans New England Clam Chowder” Due to Possible Undeclared Crab Allergen, U.S. Food & Drug Administration (FDA)
• Recall expanded to include: Raspberry Lemonade OxyELITE Pro Super Thermo Powder, U.S. Food & Drug Administration (FDA)
• Planifique un Día de Acción de Gracias libre de riesgos para su salud, GobiernoUSA.gov
• Medical Device Safety and Recalls: Medtronic Interventional Guidewires and ATTAIN HYBRID® Guidewires, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Food Safety Modernization Act and Animal Feed Update, U.S. Food & Drug Administration (FDA)
• Fossil Fuel Products, LLC, Issues Voluntary Nationwide Recall of “RezzRX” Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Jobbers Wholesale Issues Voluntary Recall of Rhino 5 Plus, Maxtremezen and Extenzone Marketed as a Dietary Supplement Due to the Presence of Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Consejos para ahorrar energía durante el invierno, GobiernoUSA.gov
• New Reliance Traders, Inc.- Voluntarily Recalls Hashmi Surma Special Eyeliner Due to Elevated Lead Levels, U.S. Food & Drug Administration (FDA)
• S&M Enterprise Issues Allergy Alert for Fruit of Wolfberry, 12 Oz Plastic Bag due to Undeclared Sulfites, U.S. Food & Drug Administration (FDA)
• Nature's Pharmacy and Compounding Center Issues Voluntary Recall of All Sterile Compounded Products Distributed Within North Carolina Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• La Boulange Cafe & Bakery Issues an Allergy Alert for Undeclared Allergen (Hazelnut) in Product Inadvertently Mislabeled as Soft Caramel Jam, U.S. Food & Drug Administration (FDA)
• FDA Classifies Medtronic's Worldwide Voluntary Field Action on Guidewires as Class I Recall, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nature's Pharmacy and Compounding Center Sterile Compounded Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Medtronic Guidewires: Recall - Potential For Coating On Surface To Delaminate And Detach, FDA MedWatch
• FDA MedWatch - October 2013 Safety Labeling Changes includes 68 products with revisions to Prescribing Information, FDA MedWatch
• Dele una mano al medio ambiente, GobiernoUSA.gov
• Vitality Research Labs, LLC, Issues Immediate Voluntary Nationwide Recall of "VitaliKOR Fast Acting" Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Crunch Pak Issues Voluntary Recall of Limited Quantities of Crunch Pak Brand Apple Slices Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 13, 2013, U.S. Food & Drug Administration (FDA)
• The November 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves medical device to treat epilepsy, U.S. Food & Drug Administration (FDA)
• Bailey's Choice Recalls Chicken Treats Because of Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• 3 Fellers LLC Issues an Allergy Alert for Undeclared Allergen (Almonds) in Chocolate Cream Pies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Over-the-Counter Topical Antiseptic Products: Drug Safety Communication - FDA Requests Label Changes and Single-Use Packaging to Decrease Risk of Infection, FDA MedWatch
• Update of CVM's What's New - Public Meeting Agenda: FSMA Proposed Rule for Preventive Controls for Animal Food, U.S. Food & Drug Administration (FDA)
• FDA approves Imbruvica for rare blood cancer, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Atossa Genetics Mammary Aspiration Specimen Cytology Test (MASCT) System Kit and the ForeCYTE Breast Health Test, U.S. Food & Drug Administration (FDA)
• Whole Foods Market® Recalls Ready-To-Eat Grain Salads, U.S. Food & Drug Administration (FDA)
• Vega Issues Voluntary Withdrawal of Vega One Nutritional Shakes and Vega Sport Performance Protein Product Due to Traces of the Antibiotic Chloramphenicol, U.S. Food & Drug Administration (FDA)
• Plum Organics Voluntarily Recalls a Range of Pouch Products, U.S. Food & Drug Administration (FDA)
• USPlabs LLC Announces a Recall of OxyElite Pro Dietary Supplements Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Palmer Candy Company Voluntarily Recalls HyVee Chocolate Caramel Clusters and HyVee Chocolate Covered Caramels Due to Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• Atherstone Foods Voluntarily Recalls Salads and Wraps Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - OxyElite Pro Dietary Supplements by USP Labs: Recall - Products Linked to Liver Illnesses, FDA MedWatch
• USPlabs LLC recalls OxyElite Pro dietary supplements; products linked to liver illnesses, U.S. Food & Drug Administration (FDA)
• Celebre el Día de los Veteranos, GobiernoUSA.gov
• Medical Device Safety and Recalls: Pentax Medical Company, PENTAX Gas/Water Valve, Model OF-B194, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baylis Medical TorFlex Transseptal Guiding Sheath Kit, U.S. Food & Drug Administration (FDA)
• FDA approves first generic versions of Aciphex delayed-release tablets to treat GERD, U.S. Food & Drug Administration (FDA)
• Garden-Fresh Foods, Inc. Expands Recall Due to Potential Contamination with Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Garden-Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA takes action to speed safety information updates on generic drugs, U.S. Food & Drug Administration (FDA)
• Tenga cuidado al comprar medicinas por Internet, GobiernoUSA.gov
• Update of CVM's What's New - Bailey’s Choice Expands Product Recall of Dog Treats in Georgia, U.S. Food & Drug Administration (FDA)
• Bailey’s Choice Expands Product Recall of Dog Treats in Georgia, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 06, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baylis Medical TorFlex Transseptal Guiding Sheath Kit: Class I Recall - Sheath Could Remove Particulate, FDA MedWatch
• FDA MedWatch - Low Molecular Weight Heparins: Drug Safety Communication - Recommendations to Decrease Risk of Spinal Column Bleeding and Paralysis, FDA MedWatch
• Update of CVM's What's New - Get the Facts! Raw Pet Food Diets can be Dangerous to You and Your Pet, U.S. Food & Drug Administration (FDA)
• Gourmet Express LLC. Voluntarily Recalls 32 Ounce Packages of "Fusia Chicken Lo Mein" and 21 Ounce Packages Of “Bremer 3 Cheese Chicken” and “Bremer Garlic Shrimp" Due to Possible Undeclared Eggs, U.S. Food & Drug Administration (FDA)
• Qué hacer si es víctima del robo de identidad, GobiernoUSA.gov
• Update of CVM's What's New - Pain Medicines for Pets: Know the Risks, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Edwards Lifesciences LLC, EMBOL-X Glide Protection System: Class I Recall - Deformed Cannula Tip, FDA MedWatch
• Medical Device Safety and Recalls: Edwards Lifesciences LLC, EMBOL-X Glide Protection System, U.S. Food & Drug Administration (FDA)
• Reser’s Fine Foods, Inc. Voluntarily Expands Recall of Refrigerated Ready-to-Eat Products Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals November 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Garden-Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk Recall Class I, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Food Safety Modernization Act (FSMA) - UPDATE, U.S. Food & Drug Administration (FDA)
• FDA: Janssen Pharmaceuticals, Inc. to plead guilty and pay over $1.6 billion to resolve allegations of misbranding and filing false claims for its schizophrenia drug Risperdal, U.S. Food & Drug Administration (FDA)
• Ghiringhelli Specialty Foods Issues Voluntary Alert on Undeclared Allergens in Caesar Salad, U.S. Food & Drug Administration (FDA)
• Dutch Treat Salads, LLC Voluntarily Recalls Mexicali Dip Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Perrigo Initiates Nationwide Voluntary Product Recall of Acetaminophen Infant Suspension Liquid, 160 mg/5 mL, Due to a Potential Defect with the Co-packaged Oral Syringe, U.S. Food & Drug Administration (FDA)
• Winn-Dixie Expands Recall to Include Spinach Antipasta Salad, U.S. Food & Drug Administration (FDA)
• Winn-Dixie Issues Recall on Pre-Prepared Broccoli Crunch Salad, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Perrigo Acetaminophen Infant Suspension Liquid: Recall - Potential Defect with Co-packaged Oral Syringe, FDA MedWatch
• Cómo funciona el Gobierno de Estados Unidos, GobiernoUSA.gov
• FDA MedWatch - September 2013 Safety Labeling Changes includes 49 products with revisions to Prescribing Information, FDA MedWatch
• Cómo identificar la adicción a los juegos de azar, GobiernoUSA.gov
• Reser's, U.S. Food & Drug Administration (FDA)
• Cambio de hora este 3 de noviembre, GobiernoUSA.gov
• FDA approves Gazyva for chronic lymphocytic leukemia, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - November 1, 2013, U.S. Food & Drug Administration (FDA)
• PENTAX Medical Company Issues Voluntary Nationwide Recall of OF-B194 Gas/ Water Valve, U.S. Food & Drug Administration (FDA)
• World Class Distribution Issues Voluntary Allergy Alert On Undeclared Soy In Southwest Salad, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 30, 2013, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Presentation on the Proposed Rule for Preventive Controls for Food for Animals, U.S. Food & Drug Administration (FDA)
• FDA takes two important actions on drug shortages, U.S. Food & Drug Administration (FDA)
• Firms Initiate Secondary Recall in Response to the Expansion of Reser’s Fine Foods Recall, U.S. Food & Drug Administration (FDA)
• Garden Fresh Foods, Inc. Expands Recalls on Specific Packages of Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Changes to Incivek (telaprevir) product labeling, U.S. Food & Drug Administration (FDA)
• BI-LO Issues Recall Of Spinach Antipasti Salad In One Store, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Clarifies Use of Melengestrol Acetate in Combination with Monensin and Tylosin, and with Monensin Alone, in Animal Feed, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Hepatitis B reactivation with certain immune-suppressing and anti-cancer drugs, U.S. Food & Drug Administration (FDA)
• Tennessee and Maryland Firms Initiate Recall Based on Reser's Fine Foods Recall, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Revised draft guidance on clinical development of treatment for chronic hepatitis C, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - How to Report a Complaint about Jerky Pet Treats, U.S. Food & Drug Administration (FDA)
• Boston Salads and Prepared Foods Recalling Ready-To- Eat Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kraft Voluntarily Recalls Some Varieties of Kraft And Polly-O String Cheese And String Cheese Twists Due to Premature Spoilage, U.S. Food & Drug Administration (FDA)
• Reser's Fine Foods, Inc. Voluntarily Expands Recall of Refrigerated Ready-to-Eat Products Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves extended-release, single-entity hydrocodone product, U.S. Food & Drug Administration (FDA)
• FDA approves second brain imaging drug to help evaluate patients for Alzheimer’s disease, dementia, U.S. Food & Drug Administration (FDA)
• Cómo prevenir el envenenamiento por plomo, GobiernoUSA.gov
• CVM Updates - FDA Issues Proposed Rule under FSMA to Improve Safety of Food for Animals, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos: ¿qué ofrece y cómo puede inscribirse?, GobiernoUSA.gov
• Violencia doméstica: qué puede hacer, GobiernoUSA.gov
• Kashmir Crown Baking LLC Issues Allergy Alert on Undeclared Eggs on KCB Pista Khatie, U.S. Food & Drug Administration (FDA)
• NatureMost Laboratories Issues Allergy Alert On Undeclared (Allergen) In Product, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 09, 2013, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 16, 2013, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 23, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - MedStream Programmable Infusion Pump and Refill Kits by Codman and Shurtleff: Class 1 Recall - Drug Over Infusion, FDA MedWatch
• Update of CVM's What's New - Prevent Heartworms in Pets Year-Round, U.S. Food & Drug Administration (FDA)
• Reser’s Fine Foods, Inc. Recalls Refrigerated Ready-to-Eat Products Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA to complete phase-out of chlorofluorocarbon inhalers, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Draeger Medical Fabius Series Anesthesia Machines - Failure of Automatic Ventilation, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Codman and Shurtleff MedStream Programmable Infusion Pump and Refill Kits - Drug Over Infusion, U.S. Food & Drug Administration (FDA)
• Sunny Pine Farms Recalls Chevre Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: GE Healthcare – Engström Ventilator and Aespire View, Aisys, Avance, and Avance CS2 Anesthesia Machines, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Progress Report on Jerky Pet Treat Investigation, U.S. Food & Drug Administration (FDA)
• Price Chopper Supermarkets Recalls Coconut Custard Pies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Specialty Medicine Compounding Pharmacy Certain Unexpired Compounded Sterile Products: Recall - Particulate Matter Found in Vials, FDA MedWatch
• Medical Device Safety and Recalls: CareFusion 211, Inc., AVEA Ventilators, All Models, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: H and H Medical Corporation (formerly H and H Associates) Emergency Cricothyrotomy Kit – Cuff Balloon May Not Function as Intended, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCL Injection, USP), 75mg/30ml, Single-Dose - Preservative Free Vial Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 02, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bard LifeStent Solo Vascular Stent: Class 1 Recall - Failure to Deploy, FDA MedWatch
• Cáncer de mama: prevención y ayuda, GobiernoUSA.gov
• FDA approves Opsumit to treat pulmonary arterial hypertension, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Bard LifeStent Solo Vascular Stent - Failure to Deploy Stent, U.S. Food & Drug Administration (FDA)
• Fahman Enterprises Inc. - Recalls Pran Brand Turmeric Powder Due to Elevated Levels of Lead, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Albuterol Sulfate Inhalation Solution, 0.083 percent (Nephron Pharmaceuticals): Recall - Aseptic Processing Simulation Results, FDA MedWatch
• FDA MedWatch - St. Jude Amplatzer Atrial Septal Occluder (ASO): Safety Communication - Reports of Tissue Erosion, FDA MedWatch
• Medical Device Safety and Recalls: Rare Serious Erosion Events Associated with St. Jude Amplatzer Atrial Septal Occluder (ASO), U.S. Food & Drug Administration (FDA)
• Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals October 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Mandy Star Trading Inc. Is Issuing an Alert on Undeclared Sulfites in "Good Taste" Brand Plum, U.S. Food & Drug Administration (FDA)
• Yoder's Country Market, Inc. Issues Allergy Alert on Gift Boxes Containing 11 oz. Bags of Honey Roasted Peanuts Distributed in December 2012, U.S. Food & Drug Administration (FDA)
• Voluntary Field Corrective Action Issued for GE Healthcare’s Engström Ventilator and Aespire View, Aisys, and Avance Anesthesia Machines, U.S. Food & Drug Administration (FDA)
• Best Value, Inc., Recalls PRAN Bran Turmeric Powder Due to Elevated Levels of Lead, U.S. Food & Drug Administration (FDA)
• B. Braun Medical Inc. Issues Voluntary Nationwide Recall of Lot H3A744, 1 gram Cefepime for Injection USP and Dextrose Injection USP Due to Visible Particulate Matter, U.S. Food & Drug Administration (FDA)
• Barrel O’ Fun Snack Foods Co. Issues Allergy Alert and Recall of Safeway Snack Artist BBQ Potato Chips Due to Mislabeling and Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Turkey Hill Dairy Issues Voluntary Recall of Chocolate Peanut Butter Cup Premium Ice Cream, Fudge Ripple Premium Ice Cream, and Moose Tracks Stuff’d Frozen Dairy Dessert, U.S. Food & Drug Administration (FDA)
• Dräger issues an update on its voluntary recall of Fabius anesthesia machines, U.S. Food & Drug Administration (FDA)
• HOSPIRA ISSUES A VOLUNTARY NATIONWIDE RECALL OF ONE LOT OF METOCLOPRAMIDE INJECTION, USP, AND TWO LOTS OF ONDANSETRON INJECTION, USP, DUE TO GLASS (GLASS STRANDS) PARTICULATES CAUSED BY GLASS SUPPLIER DEFECT, U.S. Food & Drug Administration (FDA)
• OnTime Distribution Inc. Recalls PRAN brand Spice Powder TURMERIC Due To Excessive Levels of Lead, U.S. Food & Drug Administration (FDA)
• Asia Cash & Carry Inc. Recalls PRAN Brand Spice Powder Turmeric Due to Elevated Levels of Lead, U.S. Food & Drug Administration (FDA)
• B@B Trade Inc. Issues a Voluntary Recall of "Slim Fortune", "Lidiy", and "Slim Expert" weight loss Dietary Supplement, U.S. Food & Drug Administration (FDA)
• H&H Medical Corporation Issues Nationwide Recall of Emergency Cricothyrotomy Kit, U.S. Food & Drug Administration (FDA)
• ForeCYTE Breast Health Test; Mammary Aspiration Specimen Cytology Test (MASCT), U.S. Food & Drug Administration (FDA)
• Orange County Produce, LLC Recalls Bell Peppers Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCL Injection Due To The Presence Of Dark Particulate, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Engström Ventilator, Aespire View, Aisys, And Avance Anesthesia Machines: Voluntary Field Corrective Action - Potential Safety Issue, FDA MedWatch
• FDA MedWatch - Avance, Aisys And Avance CS2 Anesthesia Delivery Systems: Voluntary Field Corrective Action - Potential Safety Issue, FDA MedWatch
• FDA MedWatch - Cefepime For Injection, USP And Dextrose Injection, USP By B. Braun Medical Inc.: Recall - Visible Particulate Matter, FDA MedWatch
• FDA MedWatch - Inclusig (Ponatinib): Drug Safety Communication - Increased Reports Of Serious Blood Clots In Arteries And Veins, FDA MedWatch
• FDA MedWatch - OxyElite Pro: Health Advisory - Acute Hepatitis Illness Cases Linked to Product Use, FDA MedWatch
• FDA MedWatch - Fabius Anesthesia Machines: Recall - Did Not Pass High Voltage Test Portion Of Final Production Test, FDA MedWatch
• FDA MedWatch - Breast Health Test and the Mammary Aspiration Specimen Cytology Test (MASCT): Recall - Concerns With Instructions For Use, Promotional Claims and FDA Clearance, FDA MedWatch
• FDA MedWatch - 1% Lidocaine HCL Injection By Hospira: Recall - Presence Of Dark Particulate, FDA MedWatch
• FDA MedWatch - Emergency Cricothyrotomy Kit By H&H Medical Corporation: Recall - Defective Cuff Balloon On Endotracheal Airway, FDA MedWatch
• FDA MedWatch - Metoclopramide Injection And Ondansetron Injection by Hospira: Recall - Glass Strand Particulates Caused By Glass Supplier Defect, FDA MedWatch
• ¿Qué pasa cuando cierra el Gobierno?, GobiernoUSA.gov
• Cierre del Gobierno 2013, GobiernoUSA.gov
• FDA MedWatch - Carefusion Avea Ventilator: Recall - Underreporting Of Tidal Volume If Used In Conjunction With Neonatal Hotwire Flow Sensor, FDA MedWatch
• CVM Updates - Notification of Industry of Impacts of the Shutdown, U.S. Food & Drug Administration (FDA)
• Big Blue Fisheries, Llc Recalls All Smoked Products From All Lots, Various Sizes, in Vacuum Packaging Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Carefusion Provides Update On Voluntary Recall Of Avea® Ventilator, U.S. Food & Drug Administration (FDA)
• Afikim Electric Vehicles Issues Nationwide Recall of Breeze C Scooter, U.S. Food & Drug Administration (FDA)
• Haute Health, LLC Conducts Voluntary Nationwide Recall of All Lots Of Virilis Pro, PHUK And Prolifta Capsules Due To Undeclared Ingredients, U.S. Food & Drug Administration (FDA)
• FDA approves new drug to treat major depressive disorder, U.S. Food & Drug Administration (FDA)
• FDA approves Perjeta for neoadjuvant breast cancer treatment, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos: qué hacer si tiene Medicare, GobiernoUSA.gov
• FDA MedWatch - The Compounding Shop - UPDATE: Do Not Use Budesonide Solution, FDA MedWatch
• FDA MedWatch - Tygacil (tigecycline): Drug Safety Communication - Increased Risk of Death, FDA MedWatch
• Safeway Recalls Several Varieties of Angel Food Cake Due to Undeclared Soy and Milk Allergens, U.S. Food & Drug Administration (FDA)
• ¿Soy elegible para inscribirme en el Mercado de Seguros Médicos?, GobiernoUSA.gov
• CVM Updates - FDA Issues Guidance on Color Additives Used in Food for Animals, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 25, 2013, U.S. Food & Drug Administration (FDA)
• Nuevos beneficios para matrimonios del mismo sexo, GobiernoUSA.gov
• Mercado de Seguros Médicos y los hispanos, GobiernoUSA.gov
• Envíenos sus preguntas sobre cómo proteger el dinero, GobiernoUSA.gov
• FDA MedWatch - W.S. Badger Company Daily SPF 30 Kids & Baby Sunscreen Lotion: Recall - Microbial Contamination, FDA MedWatch
• FDA awards seven grants to stimulate development of pediatric medical devices, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arzerra (ofatumumab) and Rituxan (rituximab): Drug Safety Communication - New Boxed Warning, Recommendations to Decrease Risk of Hepatitis B Reactivation, FDA MedWatch
• W.S. Badger Company Voluntarily Recalls Select Lots of Daily SPF 30 Kids & Baby Sunscreen Lotions Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Proposes Revision to Annual Report on Antimicrobials for Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• Garden Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Specific Lots of P.F. Chang's Home Menu Pork and Leek Dumpling Frozen Appetizers Recalled Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Duragesic (fentanyl) Patches: Drug Safety Communication - Packaging Changes to Minimize Risk of Accidental Exposure, FDA MedWatch
• FDA issues final guidance on mobile medical apps, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize food products at two Virginia food companies, U.S. Food & Drug Administration (FDA)
• Semifreddi's Announces Voluntary Recall of Almond Biscotti and Chocolate Dipped Almond Biscotti for Undeclared Milk and Soy, U.S. Food & Drug Administration (FDA)
• FDA finalizes new system to identify medical devices, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baxter Dual Luer Lock Caps: Class I Recall - Presence of Loose Particulate Matter Found In Packaging, FDA MedWatch
• Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets Issues Allergy Alert on Undeclared Soy (Allergen) in Wegmans Apple Cinnamon Mini Muffins, 14 oz., U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 18, 2013, U.S. Food & Drug Administration (FDA)
• Sea voluntario en su comunidad, GobiernoUSA.gov
• Conversemos sobre cómo cuidar su dinero, GobiernoUSA.gov
• Mes de la Herencia Hispana, GobiernoUSA.gov
• Federal judge approves consent decree against Shamrock Medical Solutions Group, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA to Hold Two Additional Public Meetings on Major FSMA Proposed Rules, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartSine Technologies Samaritan 300/300P PAD Public Access Defibrillators: Recall - Power, Battery Issues, FDA MedWatch
• Qué deben hacer los conductores cuando los para un policía, GobiernoUSA.gov
• ¿Cuánto costará la cobertura del Mercado de Seguros Médicos?, GobiernoUSA.gov
• FDA approves first generic capecitabine to treat colorectal and breast cancers, U.S. Food & Drug Administration (FDA)
• FDA prohibits manufacture of FDA-regulated drugs from Ranbaxy’s Mohali, India, plant and issues import alert, U.S. Food & Drug Administration (FDA)
• Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Honey Roasted Peanuts, for Undeclared Milk and Wheat, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Bupivacaine HCL Injection, USP (2.5 MG/ML), 30 ML Single-Dose Vial and One Lot of 0.75% Bupivacaine HCL Injection, USP (7.5 MG/ML), 30 ML Single Dose Vial Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Bupivacaine HCL Injection 0.25% (2.5 MG/ML) and Bupivacaine HCL 0.75% (7.5 MG/ML), 30 ML Single-Dose Vials by Hospira, Inc.: Recall- Presence of Particulate Matter, FDA MedWatch
• FDA MedWatch - August 2013 Safety Labeling Changes includes 34 products with revisions to Prescribing Information, FDA MedWatch
• New medical device treats urinary symptoms related to enlarged prostate, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Creafuse Powder Grape and Creafuse Powder Fruit Punch: Recall - Contains DMAA, FDA MedWatch
• GE Pharma, LLC Announces a Recall of Dietary Supplement Creafuse Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Schwebel Baking Company Voluntarily Recalls Schwebel's Golden Rich Buns With Honey Due to Undeclared Eggs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Leiter's Compounding Pharmacy: Recall - Concerns of Sterility Assurance, FDA MedWatch
• Leiter's Compounding Pharmacy Issues Voluntary Nationwide Recall of Three Product Lots Due to Lack of Assurance of Sterility Concerns Related to its Independent Testing Vendor, U.S. Food & Drug Administration (FDA)
• Talenti® Gelato & Sorbetto Issues an Allergy Alert for Undeclared Allergen (Almonds) in Talenti German Chocolate Cake Gelato Pints, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 11, 2013, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Guidance on Information Recommended for Animal Food Additive Petitions, U.S. Food & Drug Administration (FDA)
• Bubbles Baking Co. Issues an Allergen Alert for Undeclared Milk and Soy in First Street Label Blueberry Muffins, 14 oz. 9 Trays/ Case and Blueberry Loaf, 16 oz. 12 Trays/Case, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Park Compounding Sterile Medication: Recall – Concerns of Sterility Assurance, FDA MedWatch
• Park Compounding: Sterile Medication Recall – Concerns of Sterility Assurance at Testing Vendor, U.S. Food & Drug Administration (FDA)
• New Safety Measures Announced for Extended-Release and Long-Acting Opioids, U.S. Food & Drug Administration (FDA)
• FDA announces safety labeling changes and postmarket study requirements for extended-release and long-acting opioid analgesics, U.S. Food & Drug Administration (FDA)
• The September 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Avella Specialty Pharmacy Issues Voluntary Nationwide Recall of Two Medications Due to Concerns of Sterility Assurance at Testing Vendor, U.S. Food & Drug Administration (FDA)
• General Mills Announces Voluntary Recall of Limited Quantity of Refrigerated Pillsbury Cinnamon Rolls With Icing, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avella Specialty Pharmacy Sterile Medications: Recall - Concerns Of Sterility Assurance At Testing Vendor, FDA MedWatch
• FDA MedWatch - Altaire Pharmaceuticals Carboxymethylcellulose Sodium 0.5 Percent Ophthalmic Solution Sold Under Wal-Mart, CVS, and Target Brands: Recall - Preservative May Not Be Effective Through Expiry, FDA MedWatch
• FDA MedWatch - MOTRIN Infants Drops Original Berry Flavor 1/2 fl oz: Recall - Particles Identified, FDA MedWatch
• FDA MedWatch - University Compounding Pharmacy Injection Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• Altaire Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 9 Lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution Sold Under Several Brands Because the Preservative May Not Be Effective Through Expiry, U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Announces Voluntary Recall of Three Lots of Concentrated MOTRIN Infants Drops Original Berry Flavor 1/2 fl oz., U.S. Food & Drug Administration (FDA)
• Updated Press Release: GoPicnic Brands Announces Voluntary Recall of Limited Quantity Vegan Meals Due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• University Compounding Pharmacy Initiates a Nationwide Voluntary Recall of Certain Pharmacy Products due to Lack of Assurance of Sterility Concerns, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Federal judge grants FDA request for consent decree with Idaho farm, U.S. Food & Drug Administration (FDA)
• Federal judge grants FDA request for consent decree with Idaho farm, U.S. Food & Drug Administration (FDA)
• Cains Foods Issues an Allergen Alert for Undeclared Milk and Egg in Olde Cape Cod Chipotle Ranch Dressing, U.S. Food & Drug Administration (FDA)
• Medaus Pharmacy Initiates a Nationwide Recall of Certain Pharmacy Products due to Questions Surrounding an Independent Third Party’s Sterility Testing, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 04, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medaus Pharmacy Sterile Compounded Products - Recall: Inability to Confirm Sterility, FDA MedWatch
• Chobani, Inc. Voluntarily Recalls Greek Yogurt Because of Product Concerns, U.S. Food & Drug Administration (FDA)
• Ayuda financiera para estudiantes, GobiernoUSA.gov
  • <Possible follow-ups>
  • Ayuda financiera para estudiantes, GobiernoUSA.gov
• Update of CVM's What's New - Hubbard Feeds Inc. Announces an Expanded Voluntary Recall of Hubbard Life Homestead FastGrow Poultry Feed in Indiana, Michigan and Illinois Due to Elevated Calcium, U.S. Food & Drug Administration (FDA)
• Hubbard Feeds Inc. Announces an Expanded Voluntary Recall of Hubbard Life Homestead FastGrow Poultry Feed in Indiana, Michigan and Illinois Due to Elevated Calcium, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos para pequeños negocios, GobiernoUSA.gov
• FDA MedWatch - Siemens MicroScan Synergies Plus And MicroScan RapID/S Plus Negative Panels: Class I Recall - False Susceptible And False Intermediate Results, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals September 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Siemens MicroScan Synergies plus® and MicroScan® rapID/S plus Negative Panels, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Medical Device Safety and Recalls: Siemens MicroScan Synergies plus® and MicroScan® rapID/S plus Negative Panels, U.S. Food & Drug Administration (FDA)
• 6 consejos para la seguridad de los jóvenes en las redes sociales, GobiernoUSA.gov
• Update of CVM's What's New - Nestlé Purina Voluntarily Recalls Limited Number of Purina ONE beyOnd Our White Meat Chicken & Whole Barley Recipe Adult Dry Dog Food Bags, U.S. Food & Drug Administration (FDA)
• Garden-fresh Foods, Inc. Recalls Spartan Fresh Selection American Potato Salad in 16 Oz. Packages Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Aminosyn II 10 percent, Sulfite-Free, Due To Foreign Particulate Matter, U.S. Food & Drug Administration (FDA)
• Premier Foods, LLC Announces The Recall Of Products Sold At Williams-Sonoma For Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Nestle Purina Voluntarily Recalls Limited Number of Purina ONE beyOnd Our White Meat Chicken and Whole Barley Recipe Adult Dry Dog Food Bags Due to a Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Wellness Pharmacy, Inc. Issues Voluntary Recall of Six Medications Due to Concerns of Sterility Assurance at Testing Vendor, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cubicin (daptomycin for injection): Recall - Glass Particulate Matter Present in Four Lots, FDA MedWatch
• FDA MedWatch - Gilenya (fingolimod) - Drug Safety Communication: Investigating Rare Brain Infection, FDA MedWatch
• FDA MedWatch - Stryker Spine: Class 1 Recall - OASYS Midline Occiput Plate, FDA MedWatch
• Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Four Lots of Cubicin (Daptomycin for Injection) 500mg in 10ml Single Use Vials Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cutting-Edge, Essential Science on Display, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Stryker Spine - OASYS Midline Occiput Plate, U.S. Food & Drug Administration (FDA)
• Amport Foods Issues Allergy Alert on Undeclared Peanuts Mislabeled as Milk Chocolate Raisins, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 28, 2013, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Animal Feed Safety System Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Goldenfeast® Inc. Recalls Bird Food Due to Possible Salmonella Contamination from Parsley, U.S. Food & Drug Administration (FDA)
• Goldenfeast® Inc. Recalls Bird Food Due to Possible Salmonella Contamination from Parsley, U.S. Food & Drug Administration (FDA)
• Wellness Pharmacy, Inc. Issues Nationwide Voluntary Recall of Certain Sterile Products due to Laboratory Results Indicating Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Hardmenstore.com Issues Voluntary Nationwide Recall of 72HP, Evil Root and Pro Power Max Due to Undeclared Sildenafil, U.S. Food & Drug Administration (FDA)
• JCB Laboratories Issues Voluntary Recall of Six Drug Product Lots Due to Concerns of Sterility Assurance at Testing Vendor, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Wellness Pharmacy, Inc. Products: Recall - Laboratory Results Indicating Microbial Contamination, FDA MedWatch
• FDA MedWatch - JCB Laboratories Products: Recall - Sterility Assurance at Testing Vendor, FDA MedWatch
• Park Pharmacy & Compounding Center is Issuing a Voluntary Recall of Two Compounded Sterile Preparations. The Recall is Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Dove Chocolate Discoveries Issues Allergy Alert on Undeclared Nuts in Dark Chocolate Covered Fruit Collection Box, U.S. Food & Drug Administration (FDA)
• Product Recall of Kroger’s Break ‘n Bake Chocolate Chip Cookie Dough Due to Peanut Butter Cup Cookie Dough Mispacked Into Chocolate Chip Cookie Dough Packages, U.S. Food & Drug Administration (FDA)
• REACTION NUTRITION, LLC issues allergy alert on undeclared milk in LIVE CLINICAL 90 CAPS, U.S. Food & Drug Administration (FDA)
• Diagnósticos de autismo en niños hispanos, GobiernoUSA.gov
• FDA MedWatch - Ortiga: Public Notification - Contains Hidden Drug Ingredient, FDA MedWatch
• Update of CVM's What's New - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Phibro Animal Health Requests Voluntary Withdraw of Application for Medicated Poultry Feed, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 21, 2013, U.S. Food & Drug Administration (FDA)
• New test system identifies 193 different yeasts and bacteria known to cause illness, U.S. Food & Drug Administration (FDA)
• Conozca más sobre el Mercado de Seguros Médicos, GobiernoUSA.gov
• Terri Lynn, Inc. Issues Allergy Alert on Possible Undeclared Peanuts in its Packages of Deluxe Mixed Nuts, U.S. Food & Drug Administration (FDA)
• Jack Rabbit Inc. Conducts Voluntary Nationwide Recall of Lot 2510 of Jack Rabbit Dietary Supplement Due to undeclared ingredient, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Reopening of Comment Period: HIV-Focused Drug Development and HIV Cure Research, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Covidien Monoject Prefill Flush Syringes: Recall - Not Subjected To AutoClave Sterilization Process Or Mismatched Syringe Tip Cap, Syringe Label, Filled Volume And Wrapper, FDA MedWatch
• Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelder Man Capsules, Esbelder Fem Capsules, and Esbelder Siloutte Capsules Vitamin Supplements Due to Potential Health Risks, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos: esté listo, GobiernoUSA.gov
• Aidapak Services Llc Initiates Voluntary Recall of Selected Pharmaceuticals Repackaged by Aidapak Services Llc Due to Potential Incorrect Labeling Aidapak Shipped Affected Products to Four States Only: Washington, Oregon, California, and Arizona, U.S. Food & Drug Administration (FDA)
• Buurma Farms, Inc. Recalls Fresh Cilantro Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Aidapak Services LLC, Selected Repackaged Pharmaceuticals by Aidapack: Recall - Potential Incorrect Labeling, FDA MedWatch
• Voluntary Recall of Limited Lots of Maple Almond Butter Jars and Chocolate Hazelnut Butter Jars, U.S. Food & Drug Administration (FDA)
• Recuerde usar el cinturón de seguridad, GobiernoUSA.gov
• FDA MedWatch - UPDATE All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance, FDA MedWatch
• Cómo ayudar a los padres a prepararse para el regreso a clases, GobiernoUSA.gov
• FDA reminds health care providers not to use sterile products from NuVision Pharmacy, U.S. Food & Drug Administration (FDA)
• ¿Están sus hijos al día con las vacunas?, GobiernoUSA.gov
• Whole Foods Market Recalls Sour Cherry and Blueberry Crostatas Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Clarification to News Release Issued on August 9th Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fluoroquinolone Antibacterial Drugs: Drug Safety Communication- Risk for Possibly Permanent Nerve Damage, FDA MedWatch
• RECALL: Dry pet food due to possible health risk, FoodSafety.gov
• Ayuda del Gobierno: conozca más, GobiernoUSA.gov
• Update of CVM's What's New: P&G Voluntarily Recalls Limited Quantity of Dry Pet Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• P&G Voluntarily Recalls Limited Quantity of Dry Pet Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 14, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Blood Sets: Recall - Instances Of Outer Wall Of Blood Bags Punctured With Piercing Pin, FDA MedWatch
• HIV/AIDS Update - Tivicay (dolutegravir), a new drug to treat HIV-1 infection approved, U.S. Food & Drug Administration (FDA)
• FDA approves new drug to treat HIV infection, U.S. Food & Drug Administration (FDA)
• La FDA aprueba nuevo medicamento para el tratamiento de la infección de VIH, U.S. Food & Drug Administration (FDA)
• El Mercado de Seguros de Salud y sus opciones, GobiernoUSA.gov
• FDA awards contract to develop promising new technology to test radiation countermeasures, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Iradimed Corporation, MRidium 3860+ Infusion Systems equipped with MRidium 1145 Dose Error Reduction System (DERS) Drug Library Kit: Class I Recall - Potential for Incorrect Recommended Infusion Rate, FDA MedWatch
• FDA announces nationwide voluntary recall of all products for sterile use from Specialty Compounding, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - July 2013 Safety Labeling Changes includes 34 products with revisions to Prescribing Information, FDA MedWatch
• Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Specialty Compounding Sterile Products: FDA Alert - Bacterial Infections - Update, FDA MedWatch
• FDA MedWatch - Specialty Compounding Sterile Products: FDA Alert - Bacterial Infections, FDA MedWatch
• The August 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Aivlosin Untitled Letter Available, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - First rapid diagnostic test to detect both HIV-1 antigen and HIV-1/2 antibodies approved, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cordis Optease Retrievable Inferior Vena Cava (IVC) Filter: Recall - Labeling Correction, FDA MedWatch
• FDA approves first rapid diagnostic test to detect both HIV-1 antigen and HIV-1/2 antibodies, U.S. Food & Drug Administration (FDA)
• Gold Star Smoked Fish Corp. Issues an Alert on Listeria in Baltic Treasures, Norwegian Style Matjes, Marinella "Delicatessnaya", Jewish Style Matjes, Traditional Russian Matjes,and Rybacka Wies Matjes Brands of Herring Fillets in Oil, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 07, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CareFusion Alaris PC unit (model 8015) with version 9.12 Keyboard Processor: Class I Recall - Potential Loss of Communication Between Main Processor and Keyboard, FDA MedWatch
• Heeren Brothers Recalls Cantaloupe Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Health and Beyond LLC Issues Voluntary Nationwide Recall of Tranquility Product Due to Product Having Traces of Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Evershing International Trading Inc. Announces Recall of Ginger Candy, U.S. Food & Drug Administration (FDA)
• CTV BEST GROUP Inc. Issues Voluntary Nationwide Recall of Dietary Supplements BEST SLIM 40 Pills LOT # 109400 EXP: Dec. 31, 2016 because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Zip International Group, LLC Recalls Baltic Sprats in Spicy Brine Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lactancia materna: ¿por qué es importante?, GobiernoUSA.gov
  • <Possible follow-ups>
  • Lactancia materna: ¿por qué es importante?, GobiernoUSA.gov
• Alerta de viaje en Yemen, GobiernoUSA.gov
• Marketplace information that meets your needs, Health Insurance Marketplace
• Update of CVM's What's New - Updated Resolved Drug Shortages, U.S. Food & Drug Administration (FDA)
• CVM Updates - Arthritis Drug for Horses and Dogs Scheduled to Return to Market, U.S. Food & Drug Administration (FDA)
• Trois Comtois Recalls Trois Comtois Morbier Cheese for Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Advertencia sobre grave sarpullido vinculado al consumo de paracetamol, GobiernoUSA.gov
• FDA MedWatch - Benztropine Mesylate Injection (Nexus Pharmaceuticals): Recall - Visible Particulate Matter, FDA MedWatch
• Nexus Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials, U.S. Food & Drug Administration (FDA)
• FDA defines “gluten-free” for food labeling, U.S. Food & Drug Administration (FDA)
• Aproveche las compras libres de impuesto, GobiernoUSA.gov
• Update of CVM's What's New - Animal Drug Approvals August 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• CVM Updates - - FDA Announces FY 2014 Animal Drug User Fee Rates for ADUFA and AGDUFA, U.S. Food & Drug Administration (FDA)
• Purity First Health Products, Inc. Issues Nationwide Recall of Specific Lots of Healthy Life Chemistry B-50, Multi-Mineral and Vitamin C Products: Due to a Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market recalls Trois Comtois Morbier cheese because of possible health risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 31, 2013, U.S. Food & Drug Administration (FDA)
• Beacon Hill Pharmacy d/b/a Rxtra Solutions Issues Voluntary Nationwide Recall of Certain Sterile Products Due to a Question of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetaminophen: Drug Safety Communication - Association with Risk of Serious Skin Reactions, FDA MedWatch
• FDA MedWatch - DePuy Orthopaedics - LPS Lower Extremity Dovetail Intercalary Component: Class 1 Recall - Potential for Fracture of Device, FDA MedWatch
• HIV/AIDS Update - Tentative approval of emtricitabine and tenofovir disoproxil fumarate tablets, 200 mg/300 mg, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • HIV/AIDS Update - Tentative approval of emtricitabine and tenofovir disoproxil fumarate tablets, 200 mg/300 mg, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Healthy Life Chemistry By Purity First B-50: FDA Health Risk Warning - Undeclared Ingredients UPDATE, FDA MedWatch
• FDA MedWatch - Beacon Hill Medical Pharmacy/Rxtra Solutions: Recall - Lack of Sterility Assurance, FDA MedWatch
• Update of CVM's What's New - FSMA Update, U.S. Food & Drug Administration (FDA)
• Cómo preparar almuerzos saludables para niños, GobiernoUSA.gov
• FDA Veterinarian - August 1, 2013, U.S. Food & Drug Administration (FDA)
• FDA announces a voluntary recall of Nova Max Blood Glucose Test Strips, U.S. Food & Drug Administration (FDA)
• Lipari Foods Recalls Wholey Peeled Cooked Tail-on 31/40 Count Shrimp Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare Nuclear Medicine Systems: Class I Recall - Serious Injuries or Deaths Could Occur, FDA MedWatch
• Voluntary Recall of Specified Lots of Nova Max® Glucose Test Strips, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nova Max Glucose Test Strips: Recall - May Report False, Abnormally High Blood Glucose Result, FDA MedWatch
• FDA MedWatch - Mefloquine Hydrochloride: Drug Safety Communication - Label Changes Due To Risk of Serious Psychiatric and Nerve Side Effects, FDA MedWatch
• Update of CVM's What's New - New Videos from CVM's International Programs Team, U.S. Food & Drug Administration (FDA)
• FDA warns consumers about health risks with Healthy Life Chemistry dietary supplement, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Healthy Life Chemistry By Purity First B-50: FDA Health Risk Warning - Undeclared Ingredients, FDA MedWatch
• Gold Star Smoked Fish Corp. Issues an Alert on Listeria in Rybacka Wies Brand Herring Fillets in Oil "Matjes Sledz w oleju", U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Strengthening Oversight of Imported Foods, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - changes to VIREAD (tenofovir DF) labeling for Hepatitis B, U.S. Food & Drug Administration (FDA)
• FDA takes step to help ensure the safety of imported food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nizoral (ketoconazole): Drug Safety Communication - Potentially Fatal Liver Injury, Risk of Drug Interactions and Adrenal Gland Problems, FDA MedWatch
• Zip International Group LLC Recalls Herring Fillet in Oil Due to Health Risk, U.S. Food & Drug Administration (FDA)
• FDA permits marketing of first U.S. test labeled for simultaneous detection of tuberculosis bacteria and resistance to the antibiotic rifampin, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 24, 2013, U.S. Food & Drug Administration (FDA)
• Ferrara Candy Company Voluntarily Issues Allergy Alert on Undeclared Peanuts and Tree Nuts in Brach’s Malted Milk Balls, U.S. Food & Drug Administration (FDA)
• Beware of Illegally Sold Diabetes Treatments, FDA Office of Women's Health
• Olam Tomato Processors, Inc. Announces Voluntary Recall of Mild and Medium Chunky Salsa Because It May Contain Large Glass Pieces, U.S. Food & Drug Administration (FDA)
• Esté al día con la información del Gobierno, GobiernoUSA.gov
• FDA MedWatch - LeMaitre Vascular, Inc., Albograft Vascular Graft: Class I Recall - Blood Leak, FDA MedWatch
• Update of CVM's What's New: FDA Amends Regulations to Remove Requirement to Destroy Viable Turtle Eggs and Live Turtles, U.S. Food & Drug Administration (FDA)
• Cuidado de animales durante un desastre, GobiernoUSA.gov
• FDA invites public input on menthol in cigarettes, U.S. Food & Drug Administration (FDA)
• FDA alerts companies to stop illegal sale of treatments for diabetes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Diabetes Treatments: FDA Alerts of Illegal Sales - Undeclared Ingredients, FDA MedWatch
• FDA MedWatch - MedStream Programmable Infusion Pump: Class 1 Recall - Malfunction In The Fill Level Sensor, FDA MedWatch
• Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelin Siloutte Te and Esbelin Siloutte Vitamin Supplement Due to Potential Health Risks, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros de Salud y los hispanos, GobiernoUSA.gov
• FDA MedWatch - Bryan Medical Tracoe Mini 3.0mm Tracheostomy Tube: Class 1 Recall - Mislabeled Packaging, FDA MedWatch
• Volcano Company, Issues Voluntary Worldwide/Nationwide Recall of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Square Mile Cider Company Announces Voluntary Recall of 2,500 Cases of Hard Cider Products, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Additional access info for July 25 webinar, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - July 25 webinar on Draft Guidance: Human Immunodeficiency Virus-1 Infection: Developing Antiretroviral Drugs for Treatment, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 17, 2013, U.S. Food & Drug Administration (FDA)
• Seguro Social: nuevo sitio móvil, GobiernoUSA.gov
• ¿Necesita un seguro médico ahora?, GobiernoUSA.gov
• Campamentos de verano: averigüe si es elegible para un crédito tributario, GobiernoUSA.gov
• Whole Foods Market’s Mid-Atlantic Region Recalls Pimiento Cheese Due to Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Hagee Foods Inc. dba Penny's Salsa Inc. Recalls Hummus Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Prevenga el cáncer de piel, GobiernoUSA.gov
• Cuatro motivos para visitar una biblioteca este verano, GobiernoUSA.gov
• Sugerencias del Gobierno para encontrar empleo, GobiernoUSA.gov
• Update of CVM's What's New - Global Animal Health Conference, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Global Animal Health Conference, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Compliance Policy Guide for Salmonella in Food for Animals, U.S. Food & Drug Administration (FDA)
• REVISED - Western Mixers Produce & Nuts, Inc. Recalls Pistachios Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA permits marketing of first brain wave test to help assess children and teens for ADHD, U.S. Food & Drug Administration (FDA)
• Hardmenstore.com Issues Voluntary Nationwide Recall of Silver Sword and Clalis at the Request of the FDA, U.S. Food & Drug Administration (FDA)
• Olde Thompson Inc. Issues a Voluntary Recall of Earth’s Pride Organics: Organic Oregano 2.2 Oz Glass Jars With Cork Closure Due to Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Due to a Class I recall by ARO Pistachio, Torn and Glasser, Inc Announces Voluntary Recall of Pistachios Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA permits marketing of quicker method for checking effectiveness of medical device steam sterilization, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic MiniMed Paradigm Insulin Infusion Sets: Class 1 Recall - Potential for Over or Under Delivery of Insulin, FDA MedWatch
• Update of CVM's What's New - New Video Available - Medicated Feed Rules for Animal Feed Manufacturers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - June 2013 Safety Labeling Changes includes 44 products with revisions to Prescribing Information, FDA MedWatch
• FDA approves new treatment for a type of late-stage lung cancer, U.S. Food & Drug Administration (FDA)
• Western Mixers Produce & Nuts, Inc. Recalls Pistachios Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Use los registros públicos de delicuentes sexuales, GobiernoUSA.gov
• ¿Quiere refinanciar su hipoteca?, GobiernoUSA.gov
  • <Possible follow-ups>
  • ¿Quiere refinanciar su hipoteca?, GobiernoUSA.gov
• Enforcement Report for July 10, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Verathon, Inc., GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 Reusable Blades: Class I Recall - Risk of Blade Tip Breakage and Premature Failure, FDA MedWatch
• Update of CVM's What's New - FDA, Justice Department takes action against Vermont dairy farm, U.S. Food & Drug Administration (FDA)
• FDA, Justice Department takes action against Vermont dairy farm, U.S. Food & Drug Administration (FDA)
• Use una carta de queja efectiva para presentar su reclamo, GobiernoUSA.gov
• Enforcement Report for July 03, 2013, U.S. Food & Drug Administration (FDA)
• The July 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New: Hubbard Feeds Inc. Announces Voluntary Recall in Indiana and Michigan Due to Potentially Elevated Calcium and Phosphorus in Medicated Poultry Feed, U.S. Food & Drug Administration (FDA)
• Hubbard Feeds Inc. Announces Voluntary Recall in Indiana and Michigan Due to Potentially Elevated Calcium and Phosphorus in Medicated Poultry Feed, U.S. Food & Drug Administration (FDA)
• Tormentas eléctricas: cómo protegerse, GobiernoUSA.gov
• FDA MedWatch - Estarylla (norgestimate and ethinyl estradiol): Recall - Report of Placebo Tablet Present in Row of Active Tablets, FDA MedWatch
• Sandoz US Announces Voluntary Nationwide Recall of One Lot of Estarylla, U.S. Food & Drug Administration (FDA)
• Crave Brothers Farmstead Cheese Recalls Les Freres Cheese Products, U.S. Food & Drug Administration (FDA)
• Somersault Snack Co. Issues Allergy Alert on a Limited Number of 1 oz. Packages of Somersault Pacific Sea Salt Distributed Solely to Target Stores in 6-count Multipacks, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Somersault Snack Co. Issues Allergy Alert On A Limited Number Of 1 Oz. Packages Of Somersault Pacific Sea Salt Distributed Solely To Target Stores In 6-count Multipacks, U.S. Food & Drug Administration (FDA)
• Celebramos el 4 de julio y grandes inventos, GobiernoUSA.gov
  • <Possible follow-ups>
  • Celebramos el 4 de Julio y grandes inventos, GobiernoUSA.gov
• Fuegos artificiales: consejos de seguridad, GobiernoUSA.gov
• HealthCare.gov: The Health Insurance Marketplace that Serves You, Health Insurance Marketplace
• Celebramos el 4 de julio y grandes inventos: el Internet, GobiernoUSA.gov
• FDA MedWatch - Olmesartan Medoxomil: Drug Safety Communication - Label Changes To Include Intestinal Problems (Sprue-Like Enteropathy), FDA MedWatch
• FDA MedWatch - RECOMBIVAX HB (Hepatitis B Vaccine (Recombinant)) Adult Formulation by Merck Sharp and Dohme Corp.: Recall - Potential For Cracked Vials, FDA MedWatch
• HEALTH Advises Consumers Not to Eat Certain Olives, U.S. Food & Drug Administration (FDA)
• Celebramos el 4 de Julio y grandes inventos: lo que ha dado de qué hablar, GobiernoUSA.gov
• Update of CVM's What's New - Letter to Veterinary Professionals – FACTREL, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Benztropine Mesylate Injection by Fresenius Kabi USA: Recall - Potential Presence Of Glass Particles, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals July 2013 Update, U.S. Food & Drug Administration (FDA)
• Fresenius Kabi USA Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials, U.S. Food & Drug Administration (FDA)
• Celebramos el 4 de Julio y grandes inventos: sumersión a fondo, GobiernoUSA.gov
• Cómo reconocer y denunciar el maltrato de niños y ancianos, GobiernoUSA.gov
• Talenti Gelato Issues Allergy Alert For Undeclared Allergen (pecans) In Toasted Almond Gelato, U.S. Food & Drug Administration (FDA)
• Harmony Chai Voluntary Recall of Concentrated Black Spiced Chai and Decaffeinated Rooibos Chai, U.S. Food & Drug Administration (FDA)
• UPDATED RELEASE #3 UPC Code Clarification Townsend Farms, Inc. Expands Voluntary Limited Lot Recall of Frozen Organic Antioxidant Blend, 3 lb. Bag, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic SynchroMed Implantable Infusion System Devices: Class 1 Recalls - Feed Through Failure, Failure of Priming Bolus, and Catheter Occlusion, FDA MedWatch
• Medtronic Issues Medical Device Notifications Regarding The Synchromed Implantable Infusion System, U.S. Food & Drug Administration (FDA)
• FDA approves the first non-hormonal treatment for hot flashes associated with menopause, U.S. Food & Drug Administration (FDA)
• RECALL: Frozen Organic Pomegranate Kernels Due to Hep A contamination, FoodSafety.gov
• Federal judge enters consent decree with Med Prep Consulting, U.S. Food & Drug Administration (FDA)
• Dolphin Intertrade Corp, U.S. Food & Drug Administration (FDA)
• Disfrute este verano con sus hijos, GobiernoUSA.gov
• FDA approves first recombinant coagulation factor IX that is specifically indicated for routine use in preventing bleeding episodes (prophylaxis), U.S. Food & Drug Administration (FDA)
• Respironics California, Inc. Recall of V60 Ventilator Designated Class I by FDA, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Tentative approval of efavirenz, lamivudine and tenofovir disoproxil fumarate tablets, U.S. Food & Drug Administration (FDA)
• FDA takes action to protect consumers from dangerous medicines sold by illegal online pharmacies, U.S. Food & Drug Administration (FDA)
• Scenic Fruit Company Recalls Woodstock Frozen Organic Pomegranate Kernels Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 26, 2013, U.S. Food & Drug Administration (FDA)
• Beneficios del Gobierno: búsqueda fácil y rápida, GobiernoUSA.gov
  • <Possible follow-ups>
  • Beneficios del Gobierno: búsqueda fácil y rápida, GobiernoUSA.gov
• CVM Updates - Availability of CVM Internal Terms for Use in Veterinary Adverse Event Reporting, U.S. Food & Drug Administration (FDA)
• Prueba del VIH, GobiernoUSA.gov
• Price Chopper Voluntarily Recalls 3 Varieties of Burst Brand Cookies, U.S. Food & Drug Administration (FDA)
• Welcome to the new HealthCare.gov, Health Insurance Marketplace
• FDA announces first decisions on new tobacco products through the substantial equivalence pathway, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Video - Safe Medicated Feed for Animal Producers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hydroxyethyl Starch Solutions: FDA Safety Communication - Boxed Warning on Increased Mortality and Severe Renal Injury and Risk of Bleeding, FDA MedWatch
• Update of CVM's What's New - New Safe Feed Webpage, U.S. Food & Drug Administration (FDA)
• Beta Labs, LTD Announces a Recall of Dietary Supplements Oxyphen, Phentalene, Phen FX, and Red Vipers Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Vibativ for hospitalized patients with bacterial pneumonia, U.S. Food & Drug Administration (FDA)
• Taylor Farms New Jersey Issues Allergy Alert on Undeclared Tree Nuts in Black Forest Ham and Cheese on a Pretzel Roll with Swiss Cheese and Country Dijon Honey Mustard, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic Xomed NIM Trivantage EMG Endotracheal Tube: Class I Recall - Cuff Leak or Cuff Deflation When Inflation Valve Cap Inappropriately Removed, FDA MedWatch
• CVM Updates - FDA Announces Grant Funding Available for Veterinary Testing Methods, U.S. Food & Drug Administration (FDA)
• DOJ News Release: The Department of Justice Files Suit Against Louisiana Pharmaceutical Company for Distributing Unapproved and Misbranded Prescription and Over-the-counter Drugs, U.S. Food & Drug Administration (FDA)
• FDA approves Plan B One-Step emergency contraceptive for use without a prescription for all women of child-bearing potential, U.S. Food & Drug Administration (FDA)
• FDA obtains waiver from European Commission to facilitate export for U.S. pharmaceutical manufacturers, U.S. Food & Drug Administration (FDA)
• Granna's LLC Voluntarily Recalls Packages of #705 Tuna Mac With Italian Blend Vegetables and Spiced Apple Rings Due to Undeclared Eggs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Respironics California, Inc. - Class 1 Recall: V60 Ventilators - Issue with software, FDA MedWatch
• FDA approves first genotyping test for patients with hepatitis C virus, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meeting on Expanded Drug Supply Chain Authorities, U.S. Food & Drug Administration (FDA)
• Garden-Fresh Foods, Inc. Voluntarily Recalls Limited Packages of Archer Farms Smoked Salmon Dip Because of Possible Mislabeling, U.S. Food & Drug Administration (FDA)
• Advance Pharmaceutical Inc. Issues Voluntary Recall of One Lot of Enteric Coated Aspirin Tablets, 81 mg, Due to Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 19, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Enteric Coated Aspirin 81 mg Tablets by Advance Pharmaceutical Inc.: Recall of One Lot - May Contain Acetaminophen 500 mg tablets, FDA MedWatch
• Oskri is Expanding the Recall of Fig Dark Chocolate Bars to Include Additional Lots. Lot: 161 through 164, U.S. Food & Drug Administration (FDA)
• Nuevo servicio informativo de USCIS en Español, GobiernoUSA.gov
• Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zyprexa Relprevv (Olanzapine Pamoate): Drug Safety Communication - FDA Investigating Two Deaths Following Injection, FDA MedWatch
• FDA MedWatch - Endologix, Inc. AFX Introducer System: Class 1 Recall - Reports Of Dilator Breaking During Procedures, FDA MedWatch
• FDA MedWatch - Cybersecurity for Medical Devices and Hospital Networks: FDA Safety Communication, FDA MedWatch
• CVM Updates - FDA Announces the Reauthorization of User Fees to Support Timely and Efficient Review of Animal Drugs and Generic Animal Drugs, U.S. Food & Drug Administration (FDA)
• Oskri Recalls “Coconut Bar Dark Chocolate”, “Coconut Bar Dark Chocolate Minis”, “Fig Dark Chocolate Bars” and “Almond Dark Chocolate Bars” Because of Undeclared Milk, U.S. Food & Drug Administration (FDA)
• See’s Candies, Inc. Issues Allergy Alert on Undeclared Nuts and Eggs in Milk and Dark Raisins, U.S. Food & Drug Administration (FDA)
• Consejos para fortalecer la relación padre-hijo, GobiernoUSA.gov
• Lipari Foods Recalls Sunflower Seeds and Snack Mixes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Vega Issues Allergy Alert on Undeclared Milk in Vega One Bars and Vega Sport Protein Bars, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2013 Safety Labeling Changes includes 40 products with revisions to Prescribing Information, FDA MedWatch
• Butterfly Bakery Issues Allergy Alert of Undeclared Walnuts, U.S. Food & Drug Administration (FDA)
• FDA approves Xgeva to treat giant cell tumor of the bone, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Expands a Nationwide Voluntary Recall to All Lots of Vecuronium Bromide for Injection, 10mg Single Use Vials Manufactured by Mustafa Nevzat (MN Pharmaceuticals), U.S. Food & Drug Administration (FDA)
• Salud de los hombres, GobiernoUSA.gov
• Update of CVM's What's New - Hartz Mountain Corporation is Voluntarily Recalling One Specific Lot of 1.2 oz. Size of Wardley Betta Fish Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Kid's Page Article, U.S. Food & Drug Administration (FDA)
• Hartz Mountain Corporation is Voluntarily Recalling One Specific Lot of 1.2 oz. Size of Wardley Betta Fish Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Verifique las cuentas de redes sociales del Gobierno, GobiernoUSA.gov
• Zydus Pharmaceuticals USA Inc. Issues Voluntary Nationwide Recall of Warfarin 2 mg Tablets, Lot MM5767, Expiration Date June 2014, Due to Oversized Tablets, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 12, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Warfarin 2 mg Tablets by Zydus Pharmaceuticals USA Inc.: Recall - Due to Oversized Tablets, FDA MedWatch
• FDA MedWatch - Symbios GOPump and GOBlock Kits: Class 1 Recall - Potential for Excessive High Flow Rates, FDA MedWatch
• Julian’s Recipe Issues Voluntary Withdrawal of European Style Pretzel Baguette Boxes at Heb Stores in Texas, U.S. Food & Drug Administration (FDA)
• Bethel Nutritional Consulting, Inc. Issues a Voluntary Recall of Weight Loss Pills “Bethel 30” Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vecuronium Bromide For Injection by Sagent Pharmaceuticals, Inc.: Recall - Elevated Impurity Result Detected, FDA MedWatch
• HIV/AIDS Update - New new FDA Guidance for Industry: Developing Antiretroviral Drugs for Treatment, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Vecuronium Bromide for Injection, 10mg Manufactured by Mustafa Nevzat (MN Pharmaceuticals) Due to Elevated Impurity Levels, U.S. Food & Drug Administration (FDA)
• Al nadar ponga en práctica medidas de seguridad, GobiernoUSA.gov
• Alderman Farms Sales Corporation Voluntarily Recalls Organic Cherry Tomatoes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The June 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: UPDATE - FDA has identified bacterial and fungal growth in samples of preservative-free (PF) methylprednisolone acetate, FDA MedWatch
• Update of CVM's What's New - Presentations Available from FDA's Data Quality Webinar Related to 2008 ADUFA Reauthorization, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 05, 2013, U.S. Food & Drug Administration (FDA)
• UPDATED RELEASE #2 Harris Teeter Lot Code and Best By Correction Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Creole and Company, LLC Issues Allergy Alert on Undeclared Milk, Soy, and Wheat in Creole Bisque, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - 2013 AAVPT/CVM Animal Drugs in Feeds Workshop, U.S. Food & Drug Administration (FDA)
• General Mills Voluntarily Recalls Single-Serve Reduced-Sugar Cinnamon Toast Crunch Bowlpak sold in Foodservice Establishments, U.S. Food & Drug Administration (FDA)
• Prime Food USA Issues an Alert On Listeria In Latis Brand Seafood Products, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - HIV Patient-Focused Drug Development Meeting: Backgrounder Document, U.S. Food & Drug Administration (FDA)
• Gromex Inc. Issues Allergy Alert on Undeclared Sulfites in Camaron Entero (Dried Whole Shrimp), U.S. Food & Drug Administration (FDA)
• Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals June 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Food Co. Recalls Gouda Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nephron Pharmaceuticals Corp. EZ Breathe Atomizer: Class 1 Recall - Washer Could Become Dislodged, FDA MedWatch
• FDA MedWatch Celebrates 20 Years and Announces the Availability of New Consumer-Friendly Reporting Form and MedWatchLearn Tool, FDA MedWatch
• Investigan nuevo brote de Hepatitis A, GobiernoUSA.gov
• Update of CVM's What's New - Updated Listings of Veterinary Feed Directive Distributor Notifications and Approved Medicated Feed Mill Licenses, U.S. Food & Drug Administration (FDA)
• Blessing Inc. Issues Voluntary Recall On 16-20 Domestic EZ Peel Shrimp, U.S. Food & Drug Administration (FDA)
• UPDATE-Salmolux Voluntarily Recalls Cold Smoked Salmon Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• International Desserts ISSUES ALLERGY ALERT ON UNDECLARED Walnuts IN Uncle Eddies Vegan Oatmeal Chocolate Cookies, U.S. Food & Drug Administration (FDA)
• 5 actividades para disfrutar el verano en familia, GobiernoUSA.gov
• Update of CVM's What's New: 2013 Advisory Action letter, U.S. Food & Drug Administration (FDA)
• A new HealthCare.gov--plus the latest info about your state, Health Insurance Marketplace
• Cheryl's Issues A Voluntary Nationwide Recall On Its 1.6 oz. Buttercream Frosted Cinnamon Pumpkin Cookies Due To Undlecared Peanuts, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 29, 2013, U.S. Food & Drug Administration (FDA)
• Educación para niños con discapacidades, en GobiernoUSA.gov, GobiernoUSA.gov
• FDA MedWatch - Olympia Pharmacy Sterile Compounded Products: Recall - Concerns About Sterility Assurance, FDA MedWatch
• FDA MedWatch - Magnesium Sulfate: Drug Safety Communication - Recommendation Against Prolonged Use in Pre-term Labor, FDA MedWatch
• Lowlite Investments, Inc. d/b/a Olympia Pharmacy Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Compounded Between December 17, 2012, and March 27, 2013, Due to Concerns About Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Limited Number Of Lightlife Farmer’s Market Veggie Burgers Recalled Due To Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Ebproduce SA de RL Recalls Fresh Thai Peppers Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves two drugs, companion diagnostic test for advanced skin cancer, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Information on How to Participate in the Data Quality Webinar Related to 2008 ADUFA Reauthorization is Now Available, U.S. Food & Drug Administration (FDA)
• Win Luck Trading Inc. Issues Allergy Alert on Undeclared Eggs in Lam Sheng Kee's Shrimp Balls, Lobster Balls and Fish Package Eggs and Fresh Fish Cakes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magnesium Sulfate Injection by Fresenius Kabi USA: Recall - Glass Particles in Vials, FDA MedWatch
• Fresenius Kabi USA Initiates Voluntary Recall of Single Lot of Magnesium Sulfate, U.S. Food & Drug Administration (FDA)
• FDA announces import of injectable nutrition drugs, U.S. Food & Drug Administration (FDA)
• Main Street Family Pharmacy, LLC Issues Voluntary Nationwide Recall of All Sterile Compounded Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections - Update, FDA MedWatch
• Salmolux Recalls Cold Smoked Salmon Products Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Eco-Cuisine Recalls Product Because of Possible Health Risk (Extended Recall), U.S. Food & Drug Administration (FDA)
• A por un verano divertido, seguro y saludable, GobiernoUSA.gov
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections, FDA MedWatch
• FDA alerts health care providers of adverse reactions associated with steroid injections from Main Street Family Pharmacy in Tennessee, U.S. Food & Drug Administration (FDA)
• Día de la Recordación - 27 de mayo, GobiernoUSA.gov
• FDA MedWatch - Cook Medical, Inc. Zilver PTX Drug-Eluting Peripheral Stent: Class 1 Recall - Complaints of Delivery System Tip Separation, FDA MedWatch
• Cuide de la salud de sus ojos, GobiernoUSA.gov
• FDA allows marketing of first A1c test labeled for diagnosing diabetes, U.S. Food & Drug Administration (FDA)
• Order a FREE Friends and Family Health Kit today!, FDA Office of Women's Health
• Manejo del estrés después de un evento traumático, GobiernoUSA.gov
• Enforcement Report for May 22, 2013, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Letter to Bovine Veterinarians – GONAbreed, U.S. Food & Drug Administration (FDA)
• Tornados en Oklahoma: Solictud de asistencia y cómo ayudar, GobiernoUSA.gov
• LL Bakery, Inc. Announces the Recall of White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish for Undeclared Milk Allergens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Methotrexate Sodium, USP Injectable Vials by Sandoz US: Recall - Particulate Matter In Vials, FDA MedWatch
• Eco-Cuisine Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sandoz US Announces Voluntary Nationwide Recall of two lots of Methotrexate Sodium, USP, Injectable Vials, 25mg/mL, 40mL vials, U.S. Food & Drug Administration (FDA)
• Precautionary Recall Issued For Pre-Packaged Texas Gulf Shrimp, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Abbott Diabetes Care: Class 1 Recall - FreeStyle InsuLinx Blood Glucose Meters - Risk of Incorrect Test Result, FDA MedWatch
• Atención: Estafadores engañan sobre el nuevo mercado de seguros médicos, GobiernoUSA.gov
• HIV/AIDS Update - Tentative approval of lamivudine and tenofovir disoproxil fumarate Tablets, 300 mg/300 mg, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Compounded Prescription Therapies By Pentec Health Inc.: Recall - Lack Of Sterility Assurance, FDA MedWatch
• Pentec Health Announces Limited Voluntary Recall of Certain Compounded Prescription Therapies for Renal Patients, U.S. Food & Drug Administration (FDA)
• FDA seeks preliminary injunction against New York fish manufacturer, U.S. Food & Drug Administration (FDA)
• Tropical Valley Foods Issues Allergy Alert on Undeclared Milk and Walnuts in Next by Nature Dark Chocolate Bananas, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Rural King Recalls Deer Corn Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Rural King Recalls Deer Corn Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Symbios Medical Products Issues Nationwide Recall of GOPump and GOBlock Kits, U.S. Food & Drug Administration (FDA)
• Cómo prepararse para los nuevos mercados de seguros médicos, GobiernoUSA.gov
• Enforcement Report for May 15, 2013, U.S. Food & Drug Administration (FDA)
• FDA approves new drug for advanced prostate cancer, U.S. Food & Drug Administration (FDA)
• Salud de las mujeres, GobiernoUSA.gov
• HIV/AIDS Update - Public Meeting on HIV Patient-Focused Drug Development and HIV Cure Research: June 14, 2013, U.S. Food & Drug Administration (FDA)
• Spring eUpdate: Pregnancy Medication Safety, Mammography Myths & More, FDA Office of Women's Health
• Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients- Expanded to Include SexVoltz 12 Capsules Bottle, SKU 626570615316., U.S. Food & Drug Administration (FDA)
• Additional Lots Added: Voluntary Nationwide Recall of 21 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)
• In Cooperation with FDA, The Compounding Shop, LLC Declares a Voluntary Recall of All Lots of Sterile Compounded Products Due to a Lack of Sterility Assurance Distributed Within its Local Market Area, U.S. Food & Drug Administration (FDA)
• Hannaford Supermarkets Issues Allergy Alert for Two Bakery Cookie Products That May Contain Undeclared Nuts, U.S. Food & Drug Administration (FDA)
• Smart & Final Expands Recall to Include Additional Production Dates; Allergy Alert - Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini, U.S. Food & Drug Administration (FDA)
• The May 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves Breo Ellipta to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
• Krinos Foods, LLC. is Expanding its April 28, 2013 Recall to Include Additional Expiration Dates Jan 01-2014 to Jun 01-2014 of Tahini Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dairy Fresh Conducts Voluntary Recall of IGA Brand “Vanilla & Chocolate” 1.75 Quart Ice Cream Because Package May Contain Undeclared Allergens (Almonds, Coconut, Soy), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bimeda-MTC Animal Health Inc. Issues Voluntary Nationwide Recall of Sterile Solutions Due to Concerns Regarding Sterility and Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pure Herbs Ltd. Issues Allergy Recall Alert on Undeclared Allergens (Milk and Soy) in Protein Extract Urgent Undeclared Allergen Labeling Recall In Pure Herbs Ltd. Protein Extract, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Mislabeled Curried Chicken Salad and Vegan Chick’n Salad Sold at the Cold Salad Bar Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Bimeda Inc. on Behalf of Manufacturer Bimeda-MTC Animal Health Inc. Issues Voluntary Nationwide Recall of Sterile Solutions Due to Concerns Regarding Sterility and Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Atriphen dietary supplement (Xymogen brand): Recall - Potential Allergic Reaction Due to Milk and Soy, FDA MedWatch
• XYMOGEN identifies allergen oversight by third-party manufacturer; issues recall of artriphen™, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 08, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - The Compounding Shop: FDA News Release - Lack of Sterility Assurance of Drug Products, FDA MedWatch
• Beneficio Adicional de Medicare, GobiernoUSA.gov
• Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• USCIS responde a sus preguntas sobre inmigración, GobiernoUSA.gov
  • <Possible follow-ups>
  • USCIS responde a sus preguntas sobre inmigración, GobiernoUSA.gov
  • USCIS responde a sus preguntas sobre inmigración, GobiernoUSA.gov
• FDA MedWatch - Medtronic: Class 1 Recall - Medtronic Deep Brain Stimulation Lead Kit and Activa Dystonia HDE Kit, FDA MedWatch
• Disfrute del sabor de la primavera, GobiernoUSA.gov
• FDA MedWatch - Covidien Surgical Stapler Reloads: FDA Safety Communication - Devices Stolen Before They Were Sterilized, FDA MedWatch
• FDA MedWatch - Cardinal Health: Class 1 Recall - Various Presource Kits Containing a Pre-Assembled Anesthesia Circuit, FDA MedWatch
• Update of CVM's What's New - Cargill’s Animal Nutrition Business Conducts Voluntary Recall of Lamb Feed, U.S. Food & Drug Administration (FDA)
• Cargill’s Animal Nutrition Business Conducts Voluntary Recall of Lamb Feed, U.S. Food & Drug Administration (FDA)
• FDA warns pregnant women to not use certain migraine prevention medicines, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Valproate Anti-Seizure Products: Drug Safety Communication - Contraindicated for Pregnant Women for Prevention of Migraine Headaches, FDA MedWatch
• FDA MedWatch - Kadcyla (ado-trastuzumab emtansine): Drug Safety Communication - Potential Medication Errors Resulting from Name Confusion, FDA MedWatch
• ¿Tiene preguntas sobre temas de inmigración?, GobiernoUSA.gov
• HIV/AIDS Update - Sustiva (efavirenz) pediatric patients labeling update, U.S. Food & Drug Administration (FDA)
• Medtronic Announces FDA Classification Of Deep Brain Stimulation Lead Cap Communication, U.S. Food & Drug Administration (FDA)
• Nestle USA Announces Voluntary Recall of Select Varieties/Production Codes of California Pizza Kitchen and DiGiorno Frozen Pizzas, U.S. Food & Drug Administration (FDA)
• American Lifestyle Issues a Worldwide Voluntary Recall of Vicerex Capsules and Black Ant Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cancellation of 2013 Windows to Regulatory Research Internship Program, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 01, 2013, U.S. Food & Drug Administration (FDA)
• ¿Qué es la discriminación en el trabajo?, GobiernoUSA.gov
• FDA MedWatch - Newport Medical Instruments, Inc., HT70 and HT70 Plus Ventilators: Class I Recall - Unit Goes Into Internal Backup Battery Sooner Than Expected, FDA MedWatch
• FDA Veterinarian - May 1, 2013, U.S. Food & Drug Administration (FDA)
• Krinos Foods, LLC. Voluntarily Recalls Tahini Jars Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Prime Food USA Issues an Alert on Listeria in Latis Brand Herring Fillet "Antalja" in Oil and Latis Brand Herring Fillet in Oil with Spices, U.S. Food & Drug Administration (FDA)
• Carson’s Deli & Bakery Issues Allergy Alert For Undeclared Allergens In Assorted Cookie Pack And Fudge Brownie Cookie, U.S. Food & Drug Administration (FDA)