FDA News Releases

• Date Index

• Consejos prácticos para no enfermarte en temporada de frío. 🧣, USAGov en Español
• 👉 Obtén cobertura médica para ti y tu familia para el 2024, USAGov en Español
• New year, new information to explore on usa.gov 🎉, USAGov
• ¿Sabías que reconocer las señales de advertencia en tu salud mental puede marcar la diferencia? 💭💚, USAGov en Español
• Happy birthday, USAGov en Español! 🎉, USAGov
• ¡Mantente informado sobre retiros del mercado y alertas de salud pública!, USAGov en Español
• 🏥 ¡Descubre cómo solicitar Medicaid y CHIP! 🔎, USAGov en Español
• Get help finding federal agencies, USAGov
• The new USA.gov is live!, USAGov
• Discover what USAGov has for you in 2023🎉, USAGov
• Happy holidays from USAGov!, USAGov
• Encuentre ayuda para asuntos de salud mental y abuso de sustancias, USAGov en Español
• ¿Necesita cobertura médica para 2023?, USAGov en Español
• Let us know what you think of beta.USA.gov, USAGov
• Explore the next version of USA.gov, USAGov
• USAGov is Your Guide to Government Benefits, USAGov
• Get Alerts to Prepare for Disasters and Emergencies, USAGov
• Thank You and Happy New Year from USAGov! 🎉, USAGov
• Follow Hispanic Heritage Month Until Oct. 15!, USAGov
• Where and How to Get the COVID-19 Vaccine, USAGov
• Children 12 and Older Can Now Be Vaccinated Against COVID-19, USAGov
• A Moment of Silence and Day of Service to Honor 9/11, USAGov
• Get the Latest Coronavirus Information From Official Government Sources, USAGov
• Recognize and Report Coronavirus-Related Scams, USAGov
• Get Informed About the Coronavirus Through Official Government Sources, USAGov
• A Moment of Silence for the Fallen on September 11, USA.gov
• Update: USAGov Contact Center Is Open, USAGov
• USAGov Contact Center Closed Due to Hurricane Dorian, USAGov
• Spring Your Clocks Forward This Sunday ⏰, USAGov
• USA.gov website available, but not being updated, USA.gov
• Food Safety Alert: CDC Advises Not to Eat Romaine Lettuce, USA.gov
• What to Know Before Voting in the Midterm Elections, USA.gov
• Get Ready to Fall Back One Hour ⏰, USA.gov
• [New Date] Stay Alert: Nationwide Emergency Test on October 3, USA.gov
• Stay Alert: Nationwide Emergency Test on September 20, USA.gov
• FDA approves first test for screening Zika virus in blood donations, U.S. Food and Drug Administration
• Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7, U.S. Food and Drug Administration
• FDA Office of Women's Health News: Join the National Mammography Day Thunderclap, U.S. Food and Drug Administration
• FDA's Color Additive News, U.S. Food and Drug Administration
• CFSAN Constituent Update: Taking a Look at the Real-World Impact of the Gluten-Free Labeling Standard, U.S. Food and Drug Administration
• FDA Announces 2017 Public Meetings and Comment Period on Reauthorization of Two Animal Drug User Fee Programs, U.S. Food and Drug Administration
• FDA Issues Final Guidance Clarifying FDA and EPA Jurisdiction over Mosquito-Related Products, U.S. Food and Drug Administration
• FDA MedWatch - Intraocular Injections of a Compounded Triamcinolone, Moxifloxacin, and Vancomycin (TMV) Formulation: FDA Statement - Case of Hemorrhagic Occlusive Retinal Vasculitis, U.S. Food and Drug Administration
• Sid Wainer & Son® Initiates Class 1 Recall for Jansal Valley® Dried Chili De Arbol Peppers, U.S. Food and Drug Administration
• Tai Foong Usa Issues Allergy Alert on Undeclared Egg in Product, U.S. Food and Drug Administration
• FDA MedWatch - CORRECTION - Infant Sleep Positioners: FDA Warning - Risk of Suffocation, U.S. Food and Drug Administration
• FDA's Cosmetics News, U.S. Food and Drug Administration
• FDA Approves NORVIR Oral Solution Label, U.S. Food and Drug Administration
• Approved Changes to the DESCOVY Label, U.S. Food and Drug Administration
• FDA MedWatch - Infant Sleep Positioners: FDA Warning - Risk of Suffocation, U.S. Food and Drug Administration
• Greencore USA, LLC Recalls Egg Salad Sandwiches, U.S. Food and Drug Administration
• Dean Dairy Conducts Voluntary Recall of Tampico® Brand Tropical Punch, U.S. Food and Drug Administration
• Antiparasitic Resistance in Cattle and Small Ruminants in the U.S., U.S. Food and Drug Administration
• Constituent Update: FDA Proposes to Extend Compliance Dates for Nutrition Facts Label Final Rules, U.S. Food and Drug Administration
• FDA Fast Facts: FDA's Support of the Hurricane Relief Effort, U.S. Food and Drug Administration
• FDA improves access to reports of adverse drug reactions, U.S. Food and Drug Administration
• FDA approves new treatment for certain advanced or metastatic breast cancers, U.S. Food and Drug Administration
• FDA MedWatch - Endovascular Graft Systems: Letter to Health Care Providers - Type III Endoleaks Associated with Use, U.S. Food and Drug Administration
• King Soopers Recalls Deli Chicken Salad Sandwich (6.8oz) Because of Possible Health Risk, U.S. Food and Drug Administration
• 09272017_PR_FDA approves first continuous glucose monitoring system for adults not requiring blood sample calibration, U.S. Food and Drug Administration
• For Immediate Release: Silver Spring Foods, Inc. Voluntarily Recalling Waterfront Bistro Tartar Sauce Due To Possible Mislabeling and Undeclared Allergen, U.S. Food and Drug Administration
• FDA Patient Network Newsletter - Wednesday, September 27, 2017, U.S. Food and Drug Administration
• Statement from FDA Commissioner Scott Gottlieb, M.D., on new efforts to encourage compounding of better quality drugs under DQSA, U.S. Food and Drug Administration
• Federal judge orders Flawless Beauty to stop distributing unapproved drugs, recall certain products, U.S. Food and Drug Administration
• FDA MedWatch - TAH-t Companion 2 Driver System and Freedom Driver System by SynCardia: Letter to Health Providers - Mortality, Neurological Adverse Event Results, U.S. Food and Drug Administration
• FDA selects participants for new digital health software precertification pilot program, U.S. Food and Drug Administration
• FDA approved changes to the EPIVIR (lamivudine) label, U.S. Food and Drug Administration
• FDA MedWatch - Bridge Occlusion Balloon Catheter Model 590-001 by Spectranetics: Class I Recall - Risk of Blocked Guidewire Lumen Preventing Balloon Utilization, U.S. Food and Drug Administration
• Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA actions to bring relief to citizens of Puerto Rico; to help the island recover its considerable and economically vital medical product manufacturing base; and to prevent critical shortages of life-saving drugs made in Puerto Rico, U.S. Food and Drug Administration
• Spectranetics Corp. Recalls Bridge Occlusion Balloon Catheter Due to Risk of Blocked Guidewire Lumen Preventing Balloon Utilization, U.S. Food and Drug Administration
• FDA conducts major global operation to protect consumers from potentially dangerous prescription drugs sold online, U.S. Food and Drug Administration
• America New York Ri Wang Food Group Issues Allergy Alert on Seafood Products, U.S. Food and Drug Administration
• FDA Drug Shortages (New and Updated), U.S. Food and Drug Administration
• Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s immediate steps to respond to Hurricane Maria and ongoing recovery efforts related to Hurricane’s Harvey and Irma, U.S. Food and Drug Administration
• Criminal and civil actions filed against Aegerion Pharmaceuticals Inc., U.S. Food and Drug Administration
• Read about Menopause, Healthy Aging and more, U.S. Food and Drug Administration
• FDA Drug Shortages (Updated), U.S. Food and Drug Administration
  • <Possible follow-ups>
  • FDA Drug Shortages (Updated), U.S. Food and Drug Administration
  • FDA Drug Shortages (Updated), U.S. Food and Drug Administration
• FDA MedWatch - Ocaliva (obeticholic acid): Drug Safety Communication - Increased Risk of Serious Liver Injury, U.S. Food and Drug Administration
• Nature Supplement Inc. Issues Voluntary Florida Recall, U.S. Food and Drug Administration
• Death Wish Coffee Co. Announces Recall, U.S. Food and Drug Administration
• Gadget Island, Inc. Dba Gear Isle Issues Recall, U.S. Food and Drug Administration
• CFSAN Constituent Update: FDA Releases Training Module for Carriers Subject to the Sanitary Transportation Rule, U.S. Food and Drug Administration
• FDA MedWatch - Opioid Addiction Medications in Patients Taking Benzodiazepines or CNS Depressants: Drug Safety Communication - Careful Medication Management Can Reduce Risks, U.S. Food and Drug Administration
• Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency's continued efforts to promote the safe adoption of medication-assisted treatment for opioid addiction, U.S. Food and Drug Administration
• FDA clears first duodenoscope with disposable distal cap, U.S. Food and Drug Administration
• FDA Drug Shortages (New), U.S. Food and Drug Administration
  • <Possible follow-ups>
  • FDA Drug Shortages (New), U.S. Food and Drug Administration
  • FDA Drug Shortages (New), U.S. Food and Drug Administration
  • FDA Drug Shortages (New), U.S. Food and Drug Administration
  • FDA Drug Shortages (New), U.S. Food and Drug Administration
  • FDA Drug Shortages (New), U.S. Food and Drug Administration
• FDA, CDC, and USDA Announce 2017 NARMS Scientific Meeting, U.S. Food and Drug Administration
• Updated MUMS Drug Designations List, U.S. Food and Drug Administration
• Let's Stay Connected!, FoodSafety.gov
• Statement from FDA Commissioner Scott Gottlieb, M.D., about crops impacted by Hurricanes Harvey and Irma and FDA’s work with farmers affected by the storms, U.S. Food and Drug Administration
• FDA Issues Draft Guidance on the Indexing of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food and Drug Administration
• FDA approves new treatment for adults with relapsed follicular lymphoma, U.S. Food and Drug Administration
• FDA permits marketing of mobile medical application for substance abuse disorder, U.S. Food and Drug Administration
• What's New at CBER, U.S. Food and Drug Administration
  • <Possible follow-ups>
  • What's New at CBER, U.S. Food and Drug Administration
• FDA MedWatch - OriGen VV28F Reinforced Dual Lumen ECMO Catheters: Recall - Potential for Separation of Extension Tube From Hub, U.S. Food and Drug Administration
• OriGen Biomedical Issues Nationwide Recall of OriGen VV28F Reinforced Dual Lumen ECMO Catheters, U.S. Food and Drug Administration
  • <Possible follow-ups>
  • OriGen Biomedical Issues Nationwide Recall of OriGen VV28F Reinforced Dual Lumen ECMO Catheters, U.S. Food and Drug Administration
• Cherry Valley Marketplace Issues Allergy Alert on Undeclared Milk Allergens in “Cherry Valley Vanilla Cupcakes” and “Cherry Valley Chocolate Cupcakes”, U.S. Food and Drug Administration
• FDA MedWatch - Diabetes Infusion Sets by Medtronic: Recall - Vent Membrane May be Susceptible to Being Blocked by Fluid, FDA MedWatch
• Medtronic Announces Voluntary Recall of Diabetes Infusion Sets, U.S. Food & Drug Administration (FDA)
• Bravo Produce Inc. Retira Maradol Papaya de Productores y Exportadores de Carica Papaya de Tecomán y Costa Alegre SPR de RL y empacadas por Frutas Selectas de Tijuana, S. de R.L. de C.V. Por posible riesgo a la salud, U.S. Food & Drug Administration (FDA)
• Coborn’s, Inc.’s Issues Recall of American Rye Bread and Caraway Rye Bread Due To Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Commissioner Addresses State Agriculture Commissioners; Announces New Steps to Enhance Collaboration with States and Ensure Farmers Are Prepared for FSMA, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Animal Drug Safety Communication: Micotil 300 User Safety Alert, U.S. Food & Drug Administration (FDA)
• Simply Fresh Foods, Inc. Issues Allergy Alert on Undeclared Milk in Single Serve Cups of San Francisco Seafood Salad Made with Greek Yogurt, U.S. Food & Drug Administration (FDA)
• Bravo Produce Inc. Recalls Maradol Papaya from Productores Y Exportadores De Carica Papaya De Tecomán Y Costa Alegre SPR of RL and Packed by Frutas Selectas De Tijuana, S. De R.L. De C.V. Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Taking Care of Your Pets During Hurricanes and Floods, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Crops Harvested from Flooded Fields, U.S. Food & Drug Administration (FDA)
• The September 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baby Organic Liquid Formula by Garden of Life: Recall - Directions For Use May Be Misinterpreted, FDA MedWatch
• Garden of Life LLC Issues Recall of Baby Organic Liquid Formula, U.S. Food & Drug Administration (FDA)
• Emergency Preparedness for Medical Devices, U.S. Food & Drug Administration (FDA)
• Product Recall By Wegmans Assorted Muffins 4 Pack, U.S. Food & Drug Administration (FDA)
• Product Recall By Wegmans Of Assorted Muffins 4 Pack, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Acknowledges Qualified Health Claim Linking Early Peanut Introduction and Reduced Risk of Developing Peanut Allergy, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Scott Gottlieb, M.D., on a new qualified health claim advising that early introduction of peanuts to certain high-risk infants may reduce risk of peanut allergy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Activase (alteplase) 100mg by Genentech: Recall - Lack of Sterility Assurance, FDA MedWatch
• Genentech Issues Voluntary Nationwide Recall of Three Lots of Activase&reg; (Alteplase)-100 mg Due to Lack of Sterility Assurance of the Sterile Water for Injection, U.S. Food & Drug Administration (FDA)
• Country Fresh Orlando LLC, Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Datascope Corp./MAQUET Recalls Intra-Aortic Balloon Pumps Due to False Blood Detection Alarm and Ingress of Fluid into the Intra-Aortic Balloon Pump, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Intra-Aortic Balloon Pumps by Datascope/MAQUET: Class I Recall - False Blood Detection Alarm, Ingress of Fluid Into Pump, FDA MedWatch
• FDA MedWatch - Kayexalate (sodium polystyrene sulfonate): Drug Safety Communication - FDA Recommends Separating Dosing, FDA MedWatch
• CFSAN Constituent Update: FDA Releases Compliance Guide for Small Businesses under FSMA Produce Safety Rule, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Hold Public Meeting to Discuss the Development of a List of Pre-DSHEA Dietary Ingredients, U.S. Food & Drug Administration (FDA)
• Wakefern Food Corp. Voluntarily Recalls ShopRite Semi-Sweet Real Chocolate Chips, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unexpired Lots of Oxytocin Compounded with Either Lactated Ringers or Lactated Ringers and Dextrose by PharMEDium - Recall - Sub-Potency, FDA MedWatch
• PharMEDium Services, LLC Issues Voluntary Nationwide Recall of all unexpired lots of Oxytocin Compounded with Either Lactated Ringers or Lactated Ringers and Dextrose Due to Sub-Potency, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alcohol Pads or Benzalkonium Chloride Antiseptic Towelettes by Foshan Flying Medical Products: FDA Alert - Lack of Sterility Assurance and Other Quality Issues, FDA MedWatch
• FDA clears mammography device with option for patient-assisted compression, U.S. Food & Drug Administration (FDA)
• Hospira Issues Voluntary Worldwide Recall For Lots of Hydromorphone HCl Injection, USP, CII, (2 mg/mL) 1mg/mL Vial, and Levophed® (Norepinephrine Bitartrate Injection, USP), 4 mg/4 mL (1 mg/mL) Vial, Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA approves Mylotarg for treatment of acute myeloid leukemia, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Federal Veterinarians at Work, U.S. Food & Drug Administration (FDA)
• Statement from Center for Drug Evaluation and Research Director Janet Woodcock regarding safety concerns related to investigational use of Keytruda in multiple myeloma, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Keytruda (pembrolizumab) in Patients with Multiple Myeloma: FDA Statement - Two Clinical Trials on Hold, FDA MedWatch
• Mid Valley Pharmaceutical LLC Issues Voluntary Recall of Doctor Manzanilla Cough & Cold and Doctor Manzanilla Allergy & Decongestant Relief Syrup Due to Potential Contamination with Burkholderia Cepacia., U.S. Food & Drug Administration (FDA)
• Lucky Mart Inc. Issues Voluntary Nationwide Recall Of Piyanping Anti-Itch Lotion Due to Incorrect Active Ingredient, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall For One Lot of Vancomycin Hydrochloride for Injection, USP, 750 mg/vial Due to The Presence of Particulate Matter Within a Single Vial, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vancomycin Hydrochloride for Injection, USP, 750 mg/vial by Hospira: Recall - Presence of Particulate Matter, FDA MedWatch
• FDA MedWatch - Doctor Manzanilla Cough & Cold and Doctor Manzanilla Allergy & Decongestant Relief Syrup: Recall - Potential Contamination with Burkholderia cepacia, FDA MedWatch
• FDA MedWatch - Piyanping Anti-Itch Lotion: Recall - Incorrect Active Ingredient, FDA MedWatch
• Rajbhog Distributors GA Inc. Issues Allergy Alert on Undeclared Almonds in JALEBI, U.S. Food & Drug Administration (FDA)
• Dedinas Franzak Enterprises Issues Allergy Alert On Undeclared Milk In "Butter Flavored Popcorn", U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Forced Air Thermal Regulating Systems: Healthcare Provider Letter - Information About Use, FDA MedWatch
• FDA approval brings first gene therapy to the United States, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Releases Sixth Chapter of Draft Guidance for the PC-Human Food Rule, U.S. Food & Drug Administration (FDA)
• FDA approves new antibacterial drug, U.S. Food & Drug Administration (FDA)
• FDA approves first U.S. treatment for Chagas disease, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Firmware Update to Address Cybersecurity Vulnerabilities Identified in Abbott's (formerly St. Jude Medical's) Implantable Cardiac Pacemakers: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Implantable Cardiac Pacemakers by Abbott (formerly St. Jude Medical): Safety Communication - Firmware Update to Address Cybersecurity Vulnerabilities, FDA MedWatch
• Update of CVM's What's New - Safety of Food Affected by Hurricanes, Flooding, and Power Outages, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zenith Alpha Thoracic Endovascular Graft by Cook Medical: Recall Correction and Removal of Specific Sizes from Market - Increased Reports of Graft Thrombosis and Occlusion in BTAI Treatment, FDA MedWatch
• Dedinas-Franzak Enterprises Issues Allergy Alert On Undeclared Milk In Big Win Butter Popcorn, U.S. Food & Drug Administration (FDA)
• Cook Medical Issues Recall Correction of Zenith Alpha™ Thoracic Endovascular Graft and Removes Specific Sizes from the Market, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s role in ensuring Americans have access to clear and consistent calorie and nutrition information; forthcoming guidance will provide greater clarity and certainty, U.S. Food & Drug Administration (FDA)
• Norovirus & E.coli Food Safety Reminders, FoodSafety.gov
• CFSAN Constituent Update: FDA Releases Compliance Guide for Small Businesses under FSMA Intentional Adulteration Rule, U.S. Food & Drug Administration (FDA)
• Recall of Certain Frozen Organic Dark Sweet Pitted Cherry Products Due to Possible Contamination by Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ninjacof and Ninjacof A: Recall - Potential Burkholderia Cepacia Contamination, FDA MedWatch
• Centurion Labs Issues Voluntary Nationwide Recall of Ninjacof (Lot # 200N1601) and Ninjacof A (Lot# 201NA1601) Products Due to Potential <em>Burkholderia Cepacia</em> Contamination, U.S. Food & Drug Administration (FDA)
• FDA Approved Changes to the Odefsey Label, U.S. Food & Drug Administration (FDA)
• Read about Pregnancy Research, Back to School and more, FDA Office of Women's Health
• Update of CVM's What's New - Ornamental Fish Drugs and You, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Launches Food Safety Plan Builder to Help Businesses Comply with FSMA Requirements, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces Guidance for Sponsors of Certain Oncology Drugs for Companion Animals, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Releases Specialized CVM-only Version of eSubmitter Tool, U.S. Food & Drug Administration (FDA)
• Bella Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of All Sterile Drug Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Drug Products by Bella Pharmaceuticals: Recall - Lack of Sterility Assurance, FDA MedWatch
• CFSAN Constituent Update - FDA Concludes Major Sampling Study of Sprouts, U.S. Food & Drug Administration (FDA)
• Vital Rx, Inc. d/b/a Atlantic Pharmacy and Compounding Issues Voluntary Nationwide Recall of all Compounded Injectable Prescription Medications Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• United Trading Inc. Issues Allergy Alert on Undeclared Sulfites in “Gazab Green Raisins (Chinese)”, U.S. Food & Drug Administration (FDA)
• FDA provides new tools for the development and proper evaluation of tests for detecting Zika virus infection, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for adults with relapsed or refractory acute lymphoblastic leukemia, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Cook Medical Inc. Recalls Zenith Alpha Thoracic Endovascular Graft for the treatment of Blunt Traumatic Aortic Injury (BTAI) Due to the Potential Formation of Thrombus Inside the Device After Implantation, U.S. Food & Drug Administration (FDA)
• Amneal Pharmaceuticals Issues Voluntary Nationwide Recall of Lorazepam Oral Concentrate, USP 2mg/mL, Due to Misprinted Dosing Droppers Supplied with the Product, U.S. Food & Drug Administration (FDA)
• Grand BK Corp. Issues Allergy Alert on Undeclared Tree Nuts (Almonds, Walnuts and Cashews) in "California Aloha Mix", U.S. Food & Drug Administration (FDA)
• Seven Sundays LLC. Recalls Vanilla Cherry Pecan Muesli Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zenith Alpha Thoracic Endovascular Graft by Cook Medical: Class I Recall - Potential Formation of Thrombus Inside Device, FDA MedWatch
• Back to School Food Safety Tips!, FoodSafety.gov
• FDA MedWatch - Lorazepam Oral Concentrate, USP 2mg/mL by Amneal Pharmaceuticals: Recall - Misprinted Dosing Droppers, FDA MedWatch
• Revisions to the GENVOYA Label Approved, U.S. Food & Drug Administration (FDA)
• Litehouse Inc. Issues Allergy Alert on Undeclared Egg In Product, U.S. Food & Drug Administration (FDA)
• Dierbergs Markets Issues Allergy Alert on Undeclared Fish (Bonito and Cod), Lobster, Crab, Shrimp, Soy and Wheat in Product, U.S. Food & Drug Administration (FDA)
• MADHAVA Natural Sweeteners Issues Allergy Alert on Undeclared Milk in its 13.8 oz. MMM... Chocolate Chip Cookie Mix, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA’s Proposes Biomass Method to Obtain Animal Antimicrobial Sales and Distribution Data based on Animal Species and Weight, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FDA’s Proposes Biomass Method to Obtain Animal Antimicrobial Sales and Distribution Data based on Animal Species and Weight, U.S. Food & Drug Administration (FDA)
• FDA warns of potential contamination in multiple brands of drugs, dietary supplements, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: All liquid products manufactured by Pharma Tech are recalled by Leader Brand, Major Pharmaceuticals, and Rugby Laboratories because they risk being contaminated with B. cepacia., U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Exercise Enforcement Discretion for the Use and Labeling of Ultrafiltered Milk in Certain Cheeses, U.S. Food & Drug Administration (FDA)
• International Laboratories, LLC Issues Voluntary Nationwide Recall of One (1) Lot of Pravastatin Sodium Tablets USP, 40mg Packaged in Bottles of 30 Tablets Due to Mislabeling NDC # 54458-925-16; Lot # 115698A, U.S. Food & Drug Administration (FDA)
• Voluntary Nationwide Recall of all Liquid Products Manufactured by Pharmatech LLC and Distributed by Leader Brand, Major Pharmaceuticals, and Rugby Laboratories Due to Possible Product Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pravastatin Sodium Tablets by International Laboratories: Recall - Mislabeling, FDA MedWatch
• FDA MedWatch -Liquid Products Manufactured by PharmaTech and Distributed by Leader Brand, Major Pharmaceuticals, and Rugby Laboratories: Recall - Possible Product Contamination, FDA MedWatch
• Update of CVM's What's New - Getting Ready for the Next Compliance Dates for FSMA Animal Foods Rule, U.S. Food & Drug Administration (FDA)
• Schnucks Bakery Issues Allergy Alert on Undeclared Pecans in German Chocolate Cake Labeled as “Schnucks Bakery Deluxe Petite Cake Chocolate Iced Yellow”, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Liquid-filled Intragastric Balloon Systems: Letter to Healthcare Providers - Potential Risks, FDA MedWatch
• FDA MedWatch - Sterile Drug Products from Vital Rx, dba Atlantic Pharmacy and Compounding: FDA Alert - Lack of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Liquid Drug Products Manufactured by PharmaTech and Distributed by Rugby Laboratories and Possibly Other Companies: FDA Advisory - Not to Use, FDA MedWatch
• The Comfy Cow Recalls Pints of Ice Cream Due To Possible E. Coli Contamination and/or High Coliform Counts, U.S. Food & Drug Administration (FDA)
• Taylor Farms Retail, Inc. Recalls Coleslaw Kits Due To Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• The August 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA to expand public education campaign to focus on prevention of youth e-cigarette use, U.S. Food & Drug Administration (FDA)
• Freshtex Produce Recalls “Valery” Brand Maradol Papayas Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Guidances Explain Certain Exemptions from FSMA, U.S. Food & Drug Administration (FDA)
• Agroson’s LLC Recalls Maradol Papaya Cavi Brand Grown and Packed by Carica De Campeche Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Datascope Corp./MAQUET Recalls Intra-Aortic Balloon Pumps Due to Risk of Valve Failure Preventing Balloon Inflation and Deflation, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Balguti Kesaria Ayurvedic Medicine: FDA Warning - High Levels Of Lead, FDA MedWatch
• FDA MedWatch -Compounded Curcumin Emulsion Product for Injection by ImprimisRx: FDA Investigation - Serious Adverse Events Associated with Use, FDA MedWatch
• Federal judge enters consent decree against outsourcing facility Isomeric Pharmacy Solutions, U.S. Food & Drug Administration (FDA)
• MAVYRET approved to treat HCV, U.S. Food & Drug Administration (FDA)
• FDA approves Mavyret for Hepatitis C, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Diocto Liquid and Diocto Syrup by Rugby Laboratories: Recall - Possible Product Contamination, FDA MedWatch
• Rugby Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup Manufactured By PharmaTech, LLC Due to Possible Product Contamination, U.S. Food & Drug Administration (FDA)
• Grande Produce emite retiro voulantrio del mercado de una cantidad limitada de Papaya "Caribeña" por un potencial de riesgo contra la salud.”, U.S. Food & Drug Administration (FDA)
• Amrita Health Foods Voluntarily Recalls Protein Bars For Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Fairway ‘‘Like No Other Market’’ ® Recalls Fairway Brand Cookies Blondie Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves first treatment for certain types of poor-prognosis acute myeloid leukemia, U.S. Food & Drug Administration (FDA)
• Grande Produce Issues Voluntary Recall of Limited Quantity of Papaya “Caribeña” Due to Potential Health Risk (Spanish Version), U.S. Food & Drug Administration (FDA)
• Commonwealth Dairy, LLC Issues Allergy Alert On Undeclared Almond In Aldi Key Lime Crunch Tilts, U.S. Food & Drug Administration (FDA)
• FDA approves treatment for chronic graft versus host disease, U.S. Food & Drug Administration (FDA)
• The AMPT Life, LLC Issues Voluntary Nationwide Recall of AMPT Coffee due to the Presence of Undeclared Active Pharmaceutical Ingredients and Undeclared Milk, U.S. Food & Drug Administration (FDA)
• What’s New for Biologics, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • What’s New for Biologics, U.S. Food & Drug Administration (FDA)
• Man of Steel Issues Voluntary Nationwide Recall of Man of Steel 1 and Man of Steel 2 Due to Tainted Supplements, U.S. Food & Drug Administration (FDA)
• Revisions to the Epclusa Label Approved, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces FY 2018 Animal Drug User Fee Rates for ADUFA and AGDUFA, U.S. Food & Drug Administration (FDA)
• FDA approves new targeted treatment for relapsed or refractory acute myeloid leukemia, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Man of Steel 1 and Man of Steel 2: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - 0.9 % Sodium Chloride Injection by ICU Medical: Recall - Presence of Particulate Matter, FDA MedWatch
• August EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Bush Brothers & Company® Recalls Certain Baked Beans in 28 Ounce Cans Due to a Can Seam Issue, U.S. Food & Drug Administration (FDA)
• Vibrant Health Products Issues Allergy Alert On Undeclared Egg In LiveGfree Gluten Free Classic Soft White Hamburger Buns, U.S. Food & Drug Administration (FDA)
• ICU Medical Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Compounded Triamicinolone and Moxifloxacin Product for Intravitreal Injection by Guardian Pharmacy Services: Alert to Health Professionals - Serious Adverse Events Reported, FDA MedWatch
• CFSAN Constituent Update - Release of Interagency Food Safety Analytics Collaboration (IFSAC) Wrap Up, Action Plan, and Webinar Materials, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cyclobenzaprine HCl and Amantadine HCl by Apace Packaging: Recall - Potential Mislabeling, FDA MedWatch
• FDA announces comprehensive regulatory plan to shift trajectory of tobacco-related disease, death, U.S. Food & Drug Administration (FDA)
• Apace Packaging LLC Issues Voluntary Nationwide Recall of Cyclobenzaprine HCL and Amantadine HCL (Lot 16710) Due to Potential Mislabeling, U.S. Food & Drug Administration (FDA)
• Grande Produce Issues Voluntary Recall of Limited Quantity of Papaya “Caribeña” Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FW: G-00822-001039, RiOTL_Billie
• Hy-Vee, Inc. Issues Allergy Alert on Undeclared Soy in Hy-Vee Brand Pizzas, U.S. Food & Drug Administration (FDA)
• FDA Investigates Multiple Salmonella Outbreak Strains Linked to Papayas, U.S. Food & Drug Administration (FDA)
• Cantrell Drug Company Issues Voluntary Nationwide Recall of All Sterile Drug Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - La Bri's Body Health Atomic and Xplode Capsules by EZ Weight Loss TX: Recall - Undeclared Drug Ingredient, FDA MedWatch
• Update of CVM's What's New - FDA Approves First Medication for Pain Control in a Food-producing Animal, U.S. Food & Drug Administration (FDA)
• EZ Weight Loss TX LLC Issues Voluntary Nationwide Recall of Atomic and Xplode Capsules Due to the Presence of Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Enhanced CVM eSubmitter Tool Released, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Updated Status of FUJIFILM Medical Systems, U.S.A., Inc. Model ED-530XT Duodenoscopes: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Penumbra Inc. Recalls 3D Revascularization Device Due to Wire Material That May Break or Separate During Use, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Oscor Recalls ATAR Reusable and Disposable Extension Cable(s) Due to Risk of Cable Separation from Connector, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Completes Review of Qualified Health Claim Petition for Macadamia Nuts and the Risk of Coronary Heart Disease, U.S. Food & Drug Administration (FDA)
• The Idaho Foodbank Recalls Coconut Beverage, Broccoli Cheddar Soup, Eggs, and Cheese Product Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ultra Shop Supplement Issues Voluntary Nationwide Recall of Super Panther 7K Due to Presence of Undeclared Sildenafil and Tadalafil, U.S. Food & Drug Administration (FDA)
• Bhu Foods Voluntarily Recalls Protein Bars for Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Summer Food Safety Tips, FoodSafety.gov
• FDA MedWatch - Penumbra 3D Revascularization Device by Penumbra: Class I Recall - Wire Material May Break or Separate During Use, FDA MedWatch
• FDA MedWatch - ED-530XT Duodenoscopes by Fujifilm: Safety Communication - Recall Issued, Updated Design and Labeling, FDA MedWatch
• FDA clears first neonatal magnetic resonance imaging device, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Scott Gottlieb, M.D., on the Funding Awards to States for FDA Food Safety Modernization Act (FSMA) Produce Safety Implementation, U.S. Food & Drug Administration (FDA)
• Garden of Light Inc. Recalls Woodstock Organic Matcha Vanilla Oats Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bestherbs Coffee LLC Issues Voluntary Nationwide Recall of New Kopi Jantan Tradisional Natural Herbs Coffee due to the Presence of Undeclared Active Pharmaceutical Ingredients and Undeclared Milk, U.S. Food & Drug Administration (FDA)
• FDA approves Vosevi for Hepatitis C, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves Vosevi for Hepatitis C, U.S. Food & Drug Administration (FDA)
• Texas Legend Foods Issues Allergy Alert on Undeclared Cheese, Milk & Egg in "Silver Star Chipotle Dip", U.S. Food & Drug Administration (FDA)
• Smoke It Low 'N Slow, FoodSafety.gov
• Statement from FDA Commissioner Scott Gottlieb, M.D., on National Academies of Sciences, Engineering, and Medicine report on pain management and prescription opioid abuse, U.S. Food & Drug Administration (FDA)
• Statement from Alberto Gutierrez, Ph.D., Director, Office of In Vitro Diagnostics and Radiological Health, FDA’s Center for Devices and Radiological Health on the status of FDA’s investigation into inaccurate results from certain lead tests, U.S. Food & Drug Administration (FDA)
• Read about Pregnancy Research, Caregiving and more, FDA Office of Women's Health
• FDA MedWatch - Sten Z and M1 Alpha Capsules by Andropharm: Recall - Contains Derivatives of Anabolic Steroids, FDA MedWatch
• Andropharm Issues Voluntary Nationwide Recall of Sten Z and M1 Alpha Due to Labeling that it Contains Derivatives of Anabolic Steroids, U.S. Food & Drug Administration (FDA)
• Sunneen Health Foods Issues Recall of Parfait Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Coborn's, Inc. Issues Recall of Incorrectly Labeled Gluten Free Chocolate Chip Bars Due To Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Biohealth Nutrition Announces the Recall of Precision Blend Cookies and Cream Product for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• The July 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for sickle cell disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Atar Extension Cables by Oscor: Recall - Cable Separating from Connector, FDA MedWatch
• Novo Nordisk Recalls Cartridge Holders In Certain Novopen Echo® Insulin Delivery Devices Due to Potential Health Risks, U.S. Food & Drug Administration (FDA)
• Oscor Inc. Issues Nationwide Recall of ATAR Extension Cables, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Novopen Echo Insulin Delivery Device by Novo Nordisk: Recall - May Crack or Break If Exposed To Certain Chemicals, FDA MedWatch
• FDA MedWatch - Ultra-Sten and D-Zine Capsules by Hardcore Formulations: Recall - Contains Anabolic Steroids, FDA MedWatch
• Federal judge enters consent decree against Alabama compounder Medistat, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Conversation Series: Expert Insights on Protecting Consumers – Both People and Animals, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of CLIF BUILDER'S Bar Chocolate Mint Flavor, CLIF Kid Zbar Protein Chocolate Mint and CLIF Kid Zbar Protein Chocolate Chip Flavors, U.S. Food & Drug Administration (FDA)
• Hardcore Formulations Issues Voluntary Nationwide Recall of Ultra-Sten and D-Zine Capsules Due to Labeling that it Contains Anabolic Steroids, U.S. Food & Drug Administration (FDA)
• July EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Raja Foods Issues Allergy Alert on Undeclared Milk In "Anarkali Peshawari Naan Bread. Upc 0-51179-99605-2. Manufactured July 1st, 2015 Thru July 1st, 2017", U.S. Food & Drug Administration (FDA)
• Stop Food Poisoning from Crashing Your Wedding, FoodSafety.gov
• FDA clears expanded use of cooling cap to reduce hair loss during chemotherapy, U.S. Food & Drug Administration (FDA)
• Dierbergs Markets Issues Allergy Alert on Undeclared Fish and Milk in Product, U.S. Food & Drug Administration (FDA)
• Federal judge orders New York smoked fish company to stop sales due to food safety violations, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of test to aid in the detection of certain leukemias and lymphomas, U.S. Food & Drug Administration (FDA)
• What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
  • What's New at CBER Update, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Signs MOU with China to Outline Certification Process for Certain Exports, U.S. Food & Drug Administration (FDA)
• FDA unveils plan to eliminate orphan designation backlog, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Potassium Phosphate and Succinylcholine Chloride by PharMEDium Services: Recall - Lack of Sterility Assurance, FDA MedWatch
• PharMEDium Services Issues Voluntary Nationwide Recall of Specific Lots of Potassium Phosphate and Succinylcholine Chloride Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Publix Recalls Publix Tropical Medley Mix Due to Possible Contamination with Listeria monocytogenes, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Publix Recalls Publix Tropical Medley Mix Due to Possible Contamination with Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Global Lamsheng Kee Inc. Issues Allergy Alert on Undeclared Egg in Frozen Fish Tofu, Frozen Fried Fish Ball and Frozen White Fish Ball, U.S. Food & Drug Administration (FDA)
• FDA Tackles Drug Competition to Improve Patient Access, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Scott Gottlieb, M.D., on the importance of the Drug Quality and Security Act and overseeing the safety of compounded drugs, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - At FDA, a Long-term Commitment to Engaging Stakeholders, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - ADM Animal Nutrition Recalls Rough-N-Ready Cattle Feed, U.S. Food & Drug Administration (FDA)
• ADM Animal Nutrition Recalls Rough-N-Ready Cattle Feed A specific lot of product contains elevated levels of monensin, could harm cattle, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Succinylcholine Chloride 20mg/mL 5mL Syringe by Fagron Sterile Services: Recall - Potential Lack Of Sterility Assurance, FDA MedWatch
• Fagron Sterile Services Issues Voluntary Nationwide Recall of Succinylcholine Chloride Due to Potential For Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Teleflex’s (TFX) Vascular Solutions, Inc. Issues Recall of Venture® Catheters, U.S. Food & Drug Administration (FDA)
• FDA approves first subcutaneous C1 Esterase Inhibitor to treat rare genetic disease, U.S. Food & Drug Administration (FDA)
• Advanced Pharma, Inc. d/b/a Avella of Houston Issues Voluntary Nationwide Recall of Specific Lots of Potassium Phosphate and Succinylcholine Repacked and/or Compounded at its Houston Location as a Result of Hospira, Inc’s June 15, 2017 Recall of Such Products Due to a Potential Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Potassium Phosphate and Succinylcholine by Advanced Pharma: Recall - Potential Lack of Sterility Assurance, FDA MedWatch
• Medical Device Safety and Recalls: Vascular Solutions Inc. Recalls Venture Catheters due to Excess Material that May Split or Separate During Use, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Venture Catheters by Vascular Solutions: Recall - Excess Material May Split or Separate During Use, FDA MedWatch
• H-E-B Issues Recall for Undeclared Allergen. H-E-B Creamy Creations Cherry Vanilla Light Churn Style Ice Cream Being Recalled From Five Stores For Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Launches Accredited Third-Party Certification Site, U.S. Food & Drug Administration (FDA)
• JFC International Inc. Issues Missing English Label and Allergy Alert on Undeclared Wheat, Soybean, and Fish (Bonito) in Futaba Sesame Hijiki Rice Seasoning, U.S. Food & Drug Administration (FDA)
• United Natural Trading LLC Announces Voluntary Recall of Products Containing Organic and Natural Chopped Dates Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Batch of Fat Cat Purry-Purry Sauce Hot Sauce Recalled Due to Undeclared Allergens in Per-Peri Pepper Ingredient, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize adulterated food from a Minnesota warehouse, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Informs Veterinarians about Important Labeling Changes to Critical Care Medications for People, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FDA Informs Veterinarians about Important Labeling Changes to Critical Care Medications for People, U.S. Food & Drug Administration (FDA)
• Recall Expansion in New Jersey on Fewer than 650 units of Ava’s Brand Organic Roasted Unsalted Cashews and Organic Roasted Unsalted Almonds, U.S. Food & Drug Administration (FDA)
• House of Thaller Recalls Selected Pine Nut Hummus Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kabir’s Bakery issues allergy alert on undeclared milk in “Kabir’s Bakery Cinnamon Twist” and “Kabir’s Bakery Cinnamon Raisin Danish” in four ounce plastic packages, all container codes., U.S. Food & Drug Administration (FDA)
• Rikki USA, Inc. Issues Allergy Alert on Undeclared Milk in Masa’s Gourmet Sweet and Sour Sauce, Masa’s Gourmet Curry Coconut Sauce and Masa’s Gourmet Pulled Pork BBQ Sauce, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - System CS100, CS100i and CS300 Intra-Aortic Balloon Pumps by Datascope: Field Correction - Potential Electrical Test Failure Code, FDA MedWatch
• Datascope Corp/MAQUET Issues Worldwide Voluntary Recall of the System CS100, CS100i and CS300 Intra-Aortic Balloon Pumps for Potential Electrical Test Failure Code, U.S. Food & Drug Administration (FDA)
• Chic-A-Peas, LLC Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• United Pet Group Expands Voluntary Recall of Multiple Brands of Rawhide Chew Products for Dogs to Also Include Private Label Brands Due to Possible Chemical Contamination, U.S. Food & Drug Administration (FDA)
• Update to Voluntary Recall of Eliquis® (apixaban) 5 mg Tablets (#HN0063) - Recall to retail/dispensing level only, U.S. Food & Drug Administration (FDA)
• Vitakraft Sun Seed Issues Voluntary Recall of Certain Rabbit and Macaw Diets Due To Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Alvogen Issues Voluntary Nationwide Recall of Clindamycin Injection Due to a Potential for a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Clindamycin Injection ADD-Vantage Vials by Alvogen: Recall - Lack of Sterility Assurance, FDA MedWatch
• FDA recently approved changes to the Prezcobix tablet label, U.S. Food & Drug Administration (FDA)
• FDA aproved changes to the Kaletra label, U.S. Food & Drug Administration (FDA)
• NOW Health Group Inc. Expands Voluntary Recall of Ellyndale® Nutty Infusions™ Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Willis Ocean Inc Issues Alert on Uneviscerated Scomber Fish, U.S. Food & Drug Administration (FDA)
• New England Natural Bakers Issues Voluntary Recall Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut ^tm (Sodium Bicarbonate 4% Additive Solution), QUELICIN ^tm (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP Due To a Potential For Lack Of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces Minor Use/Minor Species (MUMS) Grant Application Period Due August 11, 2017, U.S. Food & Drug Administration (FDA)
• Advanced Pharma, Inc. D/B/A Avella of Houston Issues Voluntary Nationwide Recall of All Unexpired Nitroglycerin Injection In 5% Dextrose USP Products Produced At Its Houston Location From March 3, 2017 Through May 31, 2017 Due To Sub-Potency, U.S. Food & Drug Administration (FDA)
• Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Bicarbonate Injection 8.4 Percent USP, Neut (Sodium Bicarbonate 4 Percent Additive Solution), Quelicin (Succinylcholine Chloride Injection USP), and Potassium Phosphates Injection by Hospira: Recall - Potential For Lack Of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Unexpired Nitroglycerin Injection in 5 Percent Dextrose USP by Advanced Pharma in Houston: Recall - Sub Potency, FDA MedWatch
• FDA MedWatch - Paliperidone Extended-Release Tablets 3mg by Teva Pharmaceuticals: Recall - Dissolution Test Failure, FDA MedWatch
• FDA MedWatch - Frameless Stereotaxic Navigation Systems: FDA Safety Communication - Navigational Accuracy Errors, FDA MedWatch
• Statement from FDA Commissioner Scott Gottlieb, M.D., on the 2016 National Youth Tobacco Survey results, U.S. Food & Drug Administration (FDA)
• Gomacro Recalls Limited Number of Macrobars and Thrive Bars Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kroger Expands Recall of 12 oz. packages of Simple Truth Dry Roasted Macadamia Nuts because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bulletproof 360, Inc. Recalls Collagen Protein Bars and Bites Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sonar Products ordered to cease operations, Stratus Pharmaceuticals ordered to cease distributing unapproved drugs, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Navigational Accuracy Errors Associated with Frameless Stereotaxic Navigation Systems: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Read about Summer Safety and more, FDA Office of Women's Health
• Wildway LLC Issues Voluntary Recall of Certain Grain-Free Granola Products, U.S. Food & Drug Administration (FDA)
• Loving Pets Voluntarily Recalls Limited Lot Numbers of Air-Puffed Dog Treats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Loving Pets Voluntarily Recalls Limited Lot Numbers of Air-Puffed Dog Treats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Topical Products by Phillips Company: Recall - Due to Concerns of Manufacturing Practices, FDA MedWatch
• Phillips Company Issues Voluntary Worldwide Recall of All Topical Products Due to Concerns of Manufacturing Practices, U.S. Food & Drug Administration (FDA)
• Heating Things Up, FoodSafety.gov
• FDA MedWatch - Eliquis (apixaban) 5 mg tablets: Recall One Lot- Bottle labeled as Eliquis 5 mg was found to contain Eliquis 2.5 mg tablets, FDA MedWatch
• Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg Tablets, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Select Items Due to an Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• CC Kitchens Announces Recall of Limited Number of Salad and Slaw Kits Containing Leafy Greens Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Slade Gorton Co. Inc. Issues Allergy Alert On Undeclared Milk, U.S. Food & Drug Administration (FDA)
• United Pet Group Voluntary Recalls Multiple Brands of Rawhide Chew Products for Dogs Due to Possible Chemical Contamination, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - United Pet Group Voluntary Recalls Multiple Brands of Rawhide Chew Products for Dogs Due to Possible Chemical Contamination, U.S. Food & Drug Administration (FDA)
• Club Chef LLC Announces Recall of Limited Number of Snack Kits, U.S. Food & Drug Administration (FDA)
• The June 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• HIV Update: Approval of Generic Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg, U.S. Food & Drug Administration (FDA)
• FDA requests removal of Opana ER for risks related to abuse, U.S. Food & Drug Administration (FDA)
• Happy Sprout Inc. Recalls Soybean Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The FDA warns against using unapproved versions of Juvederm, FDA Office of Women's Health
• Update of CVM's What's New - Animal Drugs at FDA Phase 2 Implementation, U.S. Food & Drug Administration (FDA)
• Norvir (ritonavir) oral powder, 100 mg packet, U.S. Food & Drug Administration (FDA)
• Star Snacks Co. is voluntarily recalling two lots of Southern Grove Cashew Halves and Pieces with Sea Salt due to the potential presence of glass pieces, U.S. Food & Drug Administration (FDA)
• CORRECTION - FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna, U.S. Food & Drug Administration (FDA)
• Global Garlic Inc. Recalls "Queso Freso/Whole Milk Cheese" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Fry’s Food Stores Issues Allergy Alert on Undeclared Pecans and Tree Nuts in Bakehouse Bread Cranberry Orange Bread, U.S. Food & Drug Administration (FDA)
• FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Magellan Diagnostics Inc. Expands Recall for LeadCare Testing Systems Due to Inaccurate Test Results, U.S. Food & Drug Administration (FDA)
• FDA expands use of Sapien 3 artificial heart valve for high-risk patients, U.S. Food & Drug Administration (FDA)
• Naturally Wholesome Products LLC Wholesome Country Creamery LLC Voluntary recall of Half & Half in plastic gallon and pint bottles, due to the presence of Alkaline Phosphatase in samples, U.S. Food & Drug Administration (FDA)
• Gilster-Mary Lee Corp. Issues a Recall For Undeclared Egg Noodles in Western Family Onion Soup Mix, U.S. Food & Drug Administration (FDA)
• Schnucks Bakery Issues Allergy Alert on Undeclared Walnuts in Cinnamon Pudding Half Cakes and Cake Slices, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals June 2017 Update, U.S. Food & Drug Administration (FDA)
• Hannaford Supermarkets Issues Allergy Alert on Undeclared Milk in Taste of Inspirations Greek Pasta Salad Net. Weight 10 oz. (284g), U.S. Food & Drug Administration (FDA)
• Stay Cool on the Hiking Trail, FoodSafety.gov
• Smucker Foods of Canada Corp. Announces a Voluntary Recall on Select Golden Temple®, Swad®, and Maya® Flour Products in the U.S. Due to Possible E. Coli 0121 Contamination, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Zimmer Biomet Recalls Implantable Spinal Fusion Stimulators Due to Potential of Harmful Chemicals Which May Be Toxic to Tissues and Organs, U.S. Food & Drug Administration (FDA)
• FDA approves first generic Strattera for the treatment of ADHD, U.S. Food & Drug Administration (FDA)
• June EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Kroger Issues Allergy Alert on Undeclared Milk in Kroger Yellow Sponge Cake Dessert Cups, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Simple Truth Dry Roasted Macadamia Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas&#8482; 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas&#8482; 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information, U.S. Food & Drug Administration (FDA)
• Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle From That Lot, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulators by Zimmer Biomet: Class I Recall - Potential for Harmful Chemicals, FDA MedWatch
• CFSAN Constituent Update - FDA Sampling Finds High Level of Compliance with Gluten-Free Standards, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mibela 24 Fe Chewable Tablets by Lupin Pharmaceuticals Inc.: Recall - Out of Sequence Tablets and Missing Expiry/Lot Information, FDA MedWatch
• FDA MedWatch - Brilinta (ticagrelor) 90 mg tablets, 8-count Physician Sample Bottles: Recall of Lot # JB5047 - Due to Report of Another Medicine in One Bottle, FDA MedWatch
• Medical Device Safety and Recalls: Magellan Diagnostics Inc. Recalls LeadCare Plus and Ultra Testing Systems Due to Inaccurate Test Results, U.S. Food & Drug Administration (FDA)
• Recall on Fewer Than 225 Ava's Brand Organic Cashews Roasted & Salted 8 oz. Tubs in NJ, NY, PA and CT, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FSVP: As Compliance Date Nears, Key Facts for Importers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Caverflo Natural Herbal Coffee: Recall - Presence of Undeclared Active Pharmaceutical Ingredients, FDA MedWatch
• California Sun Dry Foods Announces a Voluntary Recall of Mislabeled California Sun Dry Sun-Dried Tomato Pesto Due to Undeclared Almond and Milk Allergen, U.S. Food & Drug Administration (FDA)
• Caverflo.com Issues Voluntary Nationwide Recall of Caverflo Natural Herbal Coffee due to the Presence of Undeclared Active Pharmaceutical Ingredients and Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Hail Merry Issues Voluntary Recall Due to Labeling Error, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Al-Er-G Capsules by MusclMasster: Recall - Contains Banned Substance Ephedra, FDA MedWatch
• Special Edition EdNet: The National Food Safety Educator's Network, FoodSafety.gov
  • <Possible follow-ups>
  • Special Edition EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Recall of Food Produced at Airway Heights Corrections Center, U.S. Food & Drug Administration (FDA)
• MusclMasster LLC Issues Voluntary Nationwide Recall of Al-Er-G Capsules Because it Contains the Banned Substance Ephedra, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Abbott-Thoratec Recalls HeartMate II LVAS Pocket System Controller Due to Risk of Patient Injury and/or Death during Backup Controller Exchange, U.S. Food & Drug Administration (FDA)
• L.A. Lucky Brand Basil Seed 2.1 oz Voluntary Recall Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartMate II LVAS Pocket System Controller by Abbott-Thoratec: CLass I Recall - Due to Risk of Patient Injury and/or Death during Backup Controller Exchange, FDA MedWatch
• FDA approves first cancer treatment for any solid tumor with a specific genetic feature, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA warns about risk of accidental overdosing of dogs with the drug Sileo, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Respironics California Recalls the V60 Non-invasive Ventilator Due to Faulty Cable Pins That May Cause the Device to Shut Down Unexpectedly, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tri-Ton by Dynamic Technical Formulations, LLC: Recall - Contains Andarine and Ostarine Drug Ingredients, FDA MedWatch
• FDA MedWatch - V60 Non-invasive Ventilator by Respironics: Class I Recall - Unexpected Device Shut Down, FDA MedWatch
• FDA MedWatch - Gadolinium-based Contrast Agents for Magnetic Resonance Imaging (MRI): Drug Safety Communication - No Harmful Effects Identified With Brain Retention, FDA MedWatch
• Dynamic Technical Formulations, LLC. Issues a Voluntary Nationwide Recall of Tri-Ton Due to the Presence of Andarine and Ostarine, U.S. Food & Drug Administration (FDA)
• BrightFarms Announces Voluntary Regional Recall of Produce Due to Potential Presence of Metal Pieces From Construction, U.S. Food & Drug Administration (FDA)
• FDA approves first drug to specifically treat giant cell arteritis, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Abbott Vascular Recalls Coronary Catheters Due to Risks Stemming from Difficulty Removing Balloon Sheath, U.S. Food & Drug Administration (FDA)
• La Nica Products, Inc. Retira Queso Por Posible Riesgo De Salud, U.S. Food & Drug Administration (FDA)
• Wang GlobalNet Issues Allergy Alert Undeclared Eggs, Wheat In “Fish Cake, Fish Ball, And Fish Tofu”, U.S. Food & Drug Administration (FDA)
• Henning’s Cheese voluntarily recalls Colby Jack cheese, U.S. Food & Drug Administration (FDA)
• Global Garlic Inc. Recalls Queso Fresco/ Whole Milk Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA expands approved use of Kalydeco to treat additional mutations of cystic fibrosis, U.S. Food & Drug Administration (FDA)
• La Nica Products, Inc. Recalls Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - LeadCare Testing Systems (with Blood Obtained from a Vein) by Magellan Diagnostics: FDA Safety Communication - Risk of Inaccurate Results, FDA MedWatch
• FDA warns Americans about risk of inaccurate results from certain lead tests, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA warns Americans about risk of inaccurate results from certain lead tests, FDA Office of Women's Health
• Medical Device Safety and Recalls: ReFlow Recalls Wingman 35 Crossing Catheters due to Tip Separation, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Coronary Catheters by Abbott: Recall - Difficulty in Removing Balloon Sheath, FDA MedWatch
• FDA MedWatch - Canagliflozin (Invokana, Invokamet): Drug Safety Communication - Increased Risk of Leg and Foot Amputations, FDA MedWatch
• Italian Gluten Free Food Cl Issues Allergy Alert On Undeclared Egg In “Chef Luca’s Lasagna Al Forno – Baked Cheese Lasagna”, U.S. Food & Drug Administration (FDA)
• Abbott Initiates Voluntarily Recall of Specific Lots of Three Coronary Catheters, U.S. Food & Drug Administration (FDA)
• Green Chile Concepts, Llc Voluntarily Recalls Select Product Codes And Production Dates Of Green Chile Food Company Brand Burrito Products, U.S. Food & Drug Administration (FDA)
• The Horton Fruit Company, Inc. Issues Voluntary Recall of Fresh Spinach Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Allergy Alert Issued by Arabella Station Whole Foods Market for Undeclared Walnuts in Oatmeal Chocolate Chip Cookies, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - CORRECTED LINKS - Looking for More Information on the Foreign Supplier Verification Programs (FSVP) Rule?, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Withdraws Draft Guidance on the Applicability of Color Additive Regulations Authorizing the Use of Certain Fruit Juice and Vegetable Juice, U.S. Food & Drug Administration (FDA)
• FDA authorizes use of new device to treat esophageal birth defect in babies, U.S. Food & Drug Administration (FDA)
• Trident Seafoods Corporation Recalls Frozen Multi-Grain Alaskan Cod Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lamb Weston Issues Allergy Alert on Undeclared Milk in Red Robin Burgers and Brews Crispy Onion Rings Sold in Grocery Stores, U.S. Food & Drug Administration (FDA)
• The May 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - UPDATED LINKS - Looking for More Information on the Foreign Supplier Verification Programs (FSVP) Rule?, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Looking for More Information on the Foreign Supplier Verification Programs (FSVP) Rule?, U.S. Food & Drug Administration (FDA)
• Mikawaya Issues Allergy Alert On Undeclared Peanuts In Limited Quantity Of Mikawaya Chocolate Chocolate Mochi Ice Cream, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets Issues Allergy Alert On Undeclared Egg In Wegmans Family Pack Food You Feel Good About Net. Weight 48 ozs. (3 LB.) 1.36 KG Potato Salad, U.S. Food & Drug Administration (FDA)
• Publix Recalls Private Label Brand of Deli Artichoke and Spinach Dip Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Quality Nut Co. Issues a Voluntary Recall, U.S. Food & Drug Administration (FDA)
• Fourth Street Barbecue/Packing Division Recalls Save-A-Lot Pick 5 Mix & Match Chicken & Waffle Sandwich Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• DIY Weddings and Food Safety, FoodSafety.gov
• Help Us Celebrate National Women’s Health Week, FDA Office of Women's Health
• Update of CVM's What's New - C.O. Truxton, Inc. Issues Voluntary Nationwide Recall of Amitriptyline HCL Tablets, USP 50mg and Phenobarbital Tablets, USP 15mg, 30mg, 60mg, 100mg Due to Potential Label Mix-Up, U.S. Food & Drug Administration (FDA)
• C.O. Truxton, Inc. Issues Voluntary Nationwide Recall of Amitriptyline HCL Tablets, USP 50mg and Phenobarbital Tablets, USP 15mg, 30mg, 60mg, 100mg Due to Potential Label Mix-Up, U.S. Food & Drug Administration (FDA)
• Pinnacle Foods Inc. Voluntarily Recalls Aunt Jemima Frozen Pancakes, Frozen Waffles & Frozen French Toast Slices Due to Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• Genetic Edge Compounds Issues Voluntary Nationwide Recall of GEC Laxoplex Dietary Supplement Capsules Due to Presence of Anabolic Steroids, U.S. Food & Drug Administration (FDA)
• Smallbatch Pets Inc. Voluntarily Recalls Frozen 2LB Chicken Blend For Dogs And Cats Due To Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GEC Laxoplex Dietary Supplement Capsules by Genetic Edge Compounds: Recall - Presence of Anabolic Steroids, FDA MedWatch
• Update of CVM's What's New - Smallbatch Pets Inc. Voluntarily Recalls Frozen 2LB Chicken Blend For Dogs And Cats Due To Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves drug to treat ALS, U.S. Food & Drug Administration (FDA)
• Herbalife International Of America, Inc. Issues Voluntary Recall For Its Protein Bar – Peanut Butter Due To Trace Amounts Of Undeclared Fish Allergen, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA takes action against Florida medicated animal feed manufacturer, U.S. Food & Drug Administration (FDA)
• Unilever Issues Allergy Alert on Undeclared Peanut in Limited Quantity of Ben & Jerry’s Chocolate Fudge Brownie Pint Slices, U.S. Food & Drug Administration (FDA)
• FDA takes action against Florida medicated animal feed manufacturer, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Mechanical Circulatory Support (formerly HeartWare Inc.) Expands Recall for Ventricular Assist Device Controllers and DC Adapter, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Recalls HeartWare Splice Kit Intended to Repair the Driveline of its Ventricular Assist Device Because it May Cause Electrical Issues or Pump Stops, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Interagency Food Safety Analytics Collaboration Webinar: Strategic Plan and Future Directions, U.S. Food & Drug Administration (FDA)
• STRIBILD and TYBOST labels have been updated, U.S. Food & Drug Administration (FDA)
• Now Health Group Inc. Voluntarily Recalls Select Ellyndale® Nutty Infusions™, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ventricular Assist Device Controllers and DC Adapter by Medtronic Mechanical Circulatory Support (formerly HeartWare Inc.): Class I Recall - Updated Controller, Power Management Software, FDA MedWatch
• U.S. Deer Antler EX. & IM., INC. Announces The Recall Of Herbal Tea Varieties In Pouches Due To Risk For Clostridium Botulinum, U.S. Food & Drug Administration (FDA)
• Imported Frozen Raw Tuna (Ahi) Cubes Distributed on Oahu Test Positive for Hepatitis A; Voluntary Product Recall Underway, U.S. Food & Drug Administration (FDA)
• ReFlow Medical Issues Recall of Specific Lots of Wingman35 Crossing Catheters, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Newport Medical Instruments Inc. Recalls Newport™ HT70 & Newport™ HT70 Plus Ventilators Due to a Software Issue which May Cause an Unexpected Shutdown without Alarm, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Wingman35 Crossing Catheters by ReFlow Medical: Recall - Tip Splitting or Separation, FDA MedWatch
• Clinical Trials Week: You Can Make a Difference, FDA Office of Women's Health
• FDA MedWatch - NavLock Tracker by Medtronic: Letter to Healthcare Providers - Patient Injuries Reported, FDA MedWatch
• CFSAN Constituent Update - FDA is Revoking Food Additive Approval for the Use of Perchlorate in Sealing Gaskets for Food Containers Because its Use Has Been Abandoned, U.S. Food & Drug Administration (FDA)
• Cosmetics News Update: Voluntary Cosmetic Registration Program Report for April 2017, U.S. Food & Drug Administration (FDA)
• May EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• CFSAN Constituent Update - FDA Extends Menu Labeling Compliance Date to 2018, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update - FDA Extends Menu Labeling Compliance Date to 2018, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2017 Update (Green Book), U.S. Food & Drug Administration (FDA)
• FDA Designates Medtronic Worldwide Voluntary Field Action on HVAD(TM) System Controllers and DC Adapters as Class I Recall, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - May 2017, U.S. Food & Drug Administration (FDA)
• FDA approves new combination treatment for acute myeloid leukemia, U.S. Food & Drug Administration (FDA)
• Phoenix Food, LLC Announces Voluntary Recall Of Dip Trio Mix Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lords Organics Recalls Ginger Powder Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Urban Remedy Issues Voluntary Recall of Mislabeled Non-Dairy Spiced Golden Milk Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - How Whole Genome Sequencing Helps Protect the Food Supply, U.S. Food & Drug Administration (FDA)
• FDA approves first treatment for a form of Batten disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - General Anesthetic and Sedation Drugs: Drug Safety Communication - FDA Approves Label Changes for Use in Young Children, FDA MedWatch
• FDA expands approved use of Stivarga to treat liver cancer, U.S. Food & Drug Administration (FDA)
• Our Local Bounty Recalls Organic Basil Pesto With Watercress Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• McCain Foods USA, Inc. Expands Voluntary Recall of Frozen Hash Browns to include Wegman’s Retail Brand Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Spring Training: Food Safety for Kids, FoodSafety.gov
• Update of CVM's What's New - FDA takes action against 14 companies for selling illegal cancer treatments, U.S. Food & Drug Administration (FDA)
• FDA takes action against 14 companies for selling illegal cancer treatments, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Illegal Cancer Treatments: FDA Warning - Fraudulent Claims of Diagnosis, Treatment, Prevention or Cure, FDA MedWatch
• Organic Herbal Supply Issues Voluntary Nationwide Recall Of All Lots Of Various Supplements For Male And Female Sexual Enhancement Due To Undeclared Active Ingredients, U.S. Food & Drug Administration (FDA)
• Party Animal Recalls Dog Food Due To Potential Presence of Pentobarbital, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Party Animal Recalls Dog Food Due To Potential Presence of Pentobarbital, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 25% Dextrose Injection, USP (Infant) by Hospira: Recall - Particulate Matter, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection, USP (Infant) Due To The Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Hummingbird Wholesale Issues Allergy Alert on Undeclared Hazelnut in Organic Cocoa-dusted Chocolate Ginger, U.S. Food & Drug Administration (FDA)
• Soylent Issues Allergy Alert On Potential Undeclared Milk in Soylent 1.8 Powder, U.S. Food & Drug Administration (FDA)
• McCain Foods USA, Inc. Recalls Frozen Southern Style Hash Browns Due to Possible Health Risk. Product is Sold and Distributed Under The Roundy’s and Harris Teeter Retail Brands., U.S. Food & Drug Administration (FDA)
• Frito-Lay Recalls Jalapeño Flavored Lay’s Kettle Cooked Potato Chips and Jalapeño Flavored Miss Vickie’s Kettle Cooked Potato Chips Due to Potential Presence of <em>Salmonella</em>, U.S. Food & Drug Administration (FDA)
• H-E-B Voluntarily Issues a Precautionary Recall H-E-B and Hill Country Fare sandwich bread with a best buy date of April 29th or earlier being recalled for potential rubber in the product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Phenobarbital 15 mg Tablets, USP by C.O. Truxton: Recall - Labeling Error on Declared Strength, FDA MedWatch
• Update of CVM's What's New - C.O. Truxton, Inc. Issues Voluntary Nationwide Recall of Phenobarbital 15 mg Tablets, USP due to Labeling Error on Declared Strength, U.S. Food & Drug Administration (FDA)
• C.O. Truxton, Inc. Issues Voluntary Nationwide Recall of Phenobarbital 15 mg Tablets, USP due to Labeling Error on Declared Strength, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Animal Drug Shortage Information, U.S. Food & Drug Administration (FDA)
• FDA Drug Safety Communication on codeine pain and cough medicines and tramadol pain medicines, FDA Office of Women's Health
• FDA statement from Douglas Throckmorton, M.D., deputy center director for regulatory programs, Center for Drug Evaluation and Research, on new warnings about the use of codeine and tramadol in children & nursing mothers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Codeine and Tramadol Medicines: Drug Safety Communication - Restricting Use in Children, Recommending Against Use in Breastfeeding Women, FDA MedWatch
• Medical Device Safety and Recalls: Medtronic Recalls StrataMR Adjustable Valves and Shunts Which May Cause Fluid Buildup in the Brain, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Advancing the Safety of Imported Food, U.S. Food & Drug Administration (FDA)
• Springtime Food Safety Tips, FoodSafety.gov
• CFSAN Constituent Update - FDA Recognizes Australia as Having a Comparable Food Safety System to the U.S., U.S. Food & Drug Administration (FDA)
• Northern California Whole Foods Market Stores Issue Recall for Undeclared Allergens in Some Cookies, U.S. Food & Drug Administration (FDA)
• Organic Herbal Supply Issue Voluntary Nationwide Recall Of All Lots Of Various Supplements For Male And Female Sexual Enhancement Due To Undeclared Tadalafil And Flibanserin, U.S. Food & Drug Administration (FDA)
• La Granja INC. Recalls Mango Flavored Ice cream Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Beyond Meat Issues Allergy Alert on Undeclared Peanut in Beyond Meat Feisty Crumbles, U.S. Food & Drug Administration (FDA)
• TP Food Processing, Inc. Announces the Recall Of Shrimp and Lemongrass Satay Sauces Due to Risk for Clostridum Botulinum, U.S. Food & Drug Administration (FDA)
• Jimmy’s Cookies LLC Issues Allergy Alert on Undeclared Milk in The Bakery Peanut Butter Chocolate Chunk Cookies LOT# 047, U.S. Food & Drug Administration (FDA)
• Read about Minority Health Month and more, FDA Office of Women's Health
• Feng Mao Biotechnology Organic Food CO.,LTD. Issues Allergy Alert on Undeclared Peanuts in Almond Drinking Powder., U.S. Food & Drug Administration (FDA)
• Northern California Whole Foods Market Stores Issue Recall for Undeclared Eggs in Some Cookies, U.S. Food & Drug Administration (FDA)
• Choice Farms LLC Recalls Limited Quantity of Caesar Side Salad Due to Undeclared Milk, Egg, Wheat and Fish (anchovies) Allergens, U.S. Food & Drug Administration (FDA)
• Standard Homeopathic Company Issues Nationwide Recall of Hyland's Baby Teething Tablets and Hyland's Baby Nighttime Teething Tablets Due to Mislabeling, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Certain Homeopathic Teething Products: Recall - Confirmed Elevated Levels of Belladonna, FDA MedWatch
• Update of CVM's What's New - Printing and Packaging CEO Pleads Guilty to Trafficking in Counterfeit Labels and Packaging, U.S. Food & Drug Administration (FDA)
• The Smokehouse of NY Recalls Smoked Fish Products Listed Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The April 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Lakeside Foods, Inc. Recalls Season's Choice Frozen Sweet Peas Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Nassau Candy Distributors Issues Allergy Alert on Undeclared Almonds in H.E.B Brand Pomegranate Infused Cranberries Covered in Dark Chocolate, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Requests Comments on Documents Related to Certain Biotechnology and Mosquito-related Products – Comment period extended, U.S. Food & Drug Administration (FDA)
• FDA approves first drug to treat tardive dyskinesia, U.S. Food & Drug Administration (FDA)
• Orthodox Baking Co Issues Allergy Alert On Undeclared Almond Paste In "Chocolate Kokosh Cake", U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Researchers to Evaluate ‘Organs-on-Chips’ Technology, U.S. Food & Drug Administration (FDA)
• Allergy Alert Issued by Whole Foods Market store in Dedham, Massachusetts for In-Store Produced Yogurt and Granola Parfaits due to Undeclared Almonds, U.S. Food & Drug Administration (FDA)
• Medtronic Announces Voluntary Worldwide Recall of its Stratamr Adjustable Valves and Shunts, U.S. Food & Drug Administration (FDA)
• Precautionary Recall of a Limited Quantity of Organic Marketside Spring Mix Salad is Announced by Fresh Express, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - StrataMR Adjustable Valves and Shunts by Medtronic: Recall - Potential for Under-Drainage of Cerebrospinal Fluid, FDA MedWatch
• Lakeside Foods, Inc. Recalls Season’s Choice Frozen Sweet Peas Because of Possible Health, U.S. Food & Drug Administration (FDA)
• FDA approves two hepatitis C drugs for pediatric patients, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves two Hepatitis C drugs for pediatric patients, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Compounded Products by Isomeric Pharmacy Solutions: Recall - Lack of Sterility Assurance, FDA MedWatch
• Isomeric Pharmacy Solutions Issues Voluntary Nationwide Recall of All Sterile Compounded Products, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of first direct-to-consumer tests that provide genetic risk information for certain conditions, U.S. Food & Drug Administration (FDA)
• In Association with Lakeside Foods, Inc., ALDI Voluntarily Recalls Season’s Choice Frozen Sweet Peas, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Explaining the FDA-State Partnership to Keep Foods Safe, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA to Hold Public Meeting in Preparation for International Cooperation on Cosmetics Regulation (ICCR-11) Meeting, U.S. Food & Drug Administration (FDA)
• 3 Ways to Celebrate Minority Health Month, FDA Office of Women's Health
• FDA MedWatch - Newport HT70 and HT70 Plus Ventilators by Medtronic: Field Corrective Action - Ventilator May Reset Spontaneously, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals April 2017 Update (Green Book), U.S. Food & Drug Administration (FDA)
• April EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Medtronic Announces Worldwide Voluntary Field Corrective Action for Newport™ HT70 and Newport™ HT70 Plus Ventilators, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Announces Three Waivers to Sanitary Transportation Rule, U.S. Food & Drug Administration (FDA)
• Olde York Issues Allergy Alert on Undeclared Milk in One Lot of Clancy’s Snack Combo 20 X 1 oz, U.S. Food & Drug Administration (FDA)
• Allergen Alert: Wegmans Food Markets, Inc. Issues Allergen Alert on Undeclared Peanuts in Wegmans Original Killer Brownies with Pecans, Sold Individually or Pre-packaged by the pound in Bakery in New York State Stores Only, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Public Alert – Dream® Plant-Based, Chocolate-Coated Frozen Desserts for Milk Allergen, U.S. Food & Drug Administration (FDA)
• Reser’s Fine Foods, Inc. Issues Allergy Alert On Undeclared Milk And Soy In Limited Quantity Of One Macaroni Salad Item, U.S. Food & Drug Administration (FDA)
• Conagra Brands Recalls Hunt’s Chili Kits Due To Potential Presence Of Salmonella In Spice Packet, U.S. Food & Drug Administration (FDA)
• Frozen Burritos Recalled Due To Possible Health Risk, Menu Del Sol Recalls Burritos in California and Nevada, U.S. Food & Drug Administration (FDA)
• Mylan Provides Update on Meridian Medical Technologies', a Pfizer Company, Expanded Voluntary Worldwide Recall of EpiPen® Auto-Injector, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - EpiPen and and EpiPen Jr Auto-Injector: Recall - Failure to Activate Device, FDA MedWatch
• FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Prelude Short Sheath Introducer by Merit Medical Systems: Class I Recall - Sheath May Separate During Use, FDA MedWatch
• Medical Device Safety and Recalls: Merit Medical Systems, Inc. Recalls the Prelude® Short Sheath Introducer - Sheath May Separate During Use, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Food Safety Modernization Act (FSMA) Updates, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Recognizes DUNS Number as Acceptable for Importer Identification, U.S. Food & Drug Administration (FDA)
• Lifestyle Evolution Voluntarily Recalls One Shift of NuGo Slim Crunchy Peanut Butter, U.S. Food & Drug Administration (FDA)
• URGENT: Envy Me Is Recalling LaBri’s Body Health Atomic 60 Capsules Due To Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Sunshine Bakery Announces Voluntary Recall of Cassava Cake And Mixed Nut Mooncake, U.S. Food & Drug Administration (FDA)
• FDA approves new drug to treat multiple sclerosis, U.S. Food & Drug Administration (FDA)
• HIV Update - Approval of fixed dose tablet containing lamivudine/zidovudine 150 mg/300 mg, U.S. Food & Drug Administration (FDA)
• FDA approves new eczema drug Dupixent, U.S. Food & Drug Administration (FDA)
• Allergy Alert Issued by Whole Foods Market in Hadley, Massachusetts For Undeclared Walnuts in Banana Chocolate Chip Muffins, U.S. Food & Drug Administration (FDA)
• FDA approves maintenance treatment for recurrent epithelial ovarian, fallopian tube or primary peritoneal cancers, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Alerts Veterinarians and Pet Food Manufacturers about Potential Presence of Thyroid Hormones in Pet Foods and Treats, U.S. Food & Drug Administration (FDA)
• Nutiva Expanded Voluntary Recall for Undeclared Peanuts In All Lots of Organic Plant Based Protein Superfood 30 Shake, U.S. Food & Drug Administration (FDA)
• Pro Sports Club Recalls Yogurt Peanut Crunch Bar Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartStart MRx Monitor/Defibrillator by Phillips Healthcare: Class I Recall - Electrical Issues, FDA MedWatch
• CFSAN Constituent Update - FDA, Federal Partners Issue New Food Safety Analytics Strategic Plan, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Phillips Healthcare recalls HeartStart MRx Monitor/Defibrillator due to electrical issues that may prevent the device from operating properly, U.S. Food & Drug Administration (FDA)
• Chlorofields Recalls Asian MIicrogreens Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves first treatment for rare form of skin cancer, U.S. Food & Drug Administration (FDA)
• Riviana Foods Inc. Voluntarily Recalls Certain Manufacturing Date And UPC Number Of Ronzoni® Thin Spaghetti Due To Possible Undeclared Egg Allergen, U.S. Food & Drug Administration (FDA)
• FDA approves drug to treat Parkinson’s disease, U.S. Food & Drug Administration (FDA)
• [New Blog] Medicines and Pregnancy: 4 Tips to Help You Get the Facts, FDA Office of Women's Health
• FDA MedWatch - Breast Implants: Update - Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL), FDA MedWatch
• EuroCan Manufacturing Voluntarily Recalling Barnsdale Farms® Pig Ears Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - EuroCan Manufacturing Voluntarily Recalling Barnsdale Farms® Pig Ears Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Nutiva Voluntary Recall for Undeclared Peanuts Organic Plant Based Protein Superfood 30 Shake Vanilla Flavor, U.S. Food & Drug Administration (FDA)
• Blue Buffalo Voluntarily Recalls One Lot of BLUE Wilderness® Rocky Mountain Recipe TM Red Meat Dinner Wet Food For Adult DogsDue to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Wellpet Voluntarily Recalls a Limited Amount of One Recipe of Canned Topper For Dogs Due to Potential Elevated Levels of Naturally Occurring Beef Thyroid Hormone, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Absorb GT1 Bioresorbable Vascular Scaffold (BVS) by Abbott Vascular: Letter to Health Care Providers - FDA Investigating Increased Rate of Major Adverse Cardiac Events, FDA MedWatch
• Aroma Imports Inc. Recalls Nabelsi brand Thyme Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Advanced Fresh Concepts Franchise Corp. Voluntarily Recalls Edamame Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Read about Women's History Month, Heart Health and more, FDA Office of Women's Health
• FDA MedWatch - Viberzi (eluxadoline): Drug Safety Communication - Increased Risk of Serious Pancreatitis In Patients Without A Gallbladder, FDA MedWatch
• Medical Device Safety and Recalls: Medtronic Recalls SynchroMed II and SynchroMed EL Implantable Drug Infusion Pumps Due to Failure of Priming Bolus – Update Related to May 2013 Recall, U.S. Food & Drug Administration (FDA)
• Dolcetta Artisan Sweets Issues Allergy Alert on Undeclared Soy and Milk in Chocolate Confections, U.S. Food & Drug Administration (FDA)
• Colorado unapproved drug and dietary supplement makers ordered to cease operations for federal violations, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SynchroMed II and SynchroMed EL Implantable Drug Infusion Pumps by Medtronic: Class I Recall - Failure of Priming Bolus, FDA MedWatch
• Whole Foods Market Expands Vulto Creamery Recall Because of Public Health Risk, U.S. Food & Drug Administration (FDA)
• Public Meeting on Patient-Focused Drug Development for Sarcopenia, FDA Office of Women's Health
• The Soynut Butter Co Expands Recall to Include Dixie U.S.A Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Vulto Creamery Voluntarily Expands Their Recall of All Raw Milk Cheeses Because of Possible Listeria Monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• A&H Focal Inc. Issues Nationwide Recall of 21 Products Marketed as Dietary Supplements & One Cosmetic Product Due to the Possible Presence of Undeclared Erectile Dysfunction Ingredients, U.S. Food & Drug Administration (FDA)
• Nonna Foods Issues Allergy Alert on Undeclared Milk in Lidia’s Marinara Sauce, U.S. Food & Drug Administration (FDA)
• Bak-Ez Issues Allergy Alert on Undeclared (Milk) in Mantecada (Muffin), U.S. Food & Drug Administration (FDA)
• Regeneca Worldwide, a Division of Vivaceuticals, Inc., Issues a Nationwide Recall of Its Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Herbal and Dietary Supplement Products by Regeneca Worldwide: Recall - Not Manufactured in Compliance with Current Good Manufacturing Practices, FDA MedWatch
• FDA MedWatch - SPS-1 Static Preservation Solution distributed by Organ Recovery Systems: Safety Communication - FDA Warns Of Potential Contamination, FDA MedWatch
• Medical Device Safety and Recalls: Physio-Control Inc. Recalls LIFEPAK 1000 Defibrillator Due to an Electrical Issue Which May Cause the Device to Shut Down Unexpectedly, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: FDA Warns Of Potentially Contaminated SPS-1 Static Preservation Solution Distributed by Organ Recovery Systems, Inc.: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Cheeses From 9 Stores Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gerber Issues Allergy Alert To Clarify Egg Labeling For Cheese Ravioli Pasta Pick-ups&reg;, U.S. Food & Drug Administration (FDA)
• Biery Cheese Company Expands Recall of Select Cheese Due To Possible Listeria Monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch -Balloon angioplasty devices to treat autonomic dysfunction: FDA Safety Communication - FDA concern over experimental procedures, FDA MedWatch
• Medical Device Safety and Recalls: FDA concern over experimental procedures that use balloon angioplasty devices to treat autonomic dysfunction: FDA safety communication, U.S. Food & Drug Administration (FDA)
• A&H Focal Inc. Issues Nationwide Recall of 29 Products Marketed as Dietary Supplements Due to The Possible Presence of Undeclared Erectile Dysfunction Ingredients, U.S. Food & Drug Administration (FDA)
• The Soynut Butter Co Expands Recall to All I.M. Healthy Soynut Butters And I.M. Healthy Granola Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)