FDA News
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- Food Safety Alert: CDC Advises Not to Eat Romaine Lettuce
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- [New Date] Stay Alert: Nationwide Emergency Test on October 3
- Stay Alert: Nationwide Emergency Test on September 20
- FDA approves first test for screening Zika virus in blood donations
- From: U.S. Food and Drug Administration
- Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7
- From: U.S. Food and Drug Administration
- FDA Office of Women's Health News: Join the National Mammography Day Thunderclap
- From: U.S. Food and Drug Administration
- FDA's Color Additive News
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (Updated)
- From: U.S. Food and Drug Administration
- What's New at CBER
- From: U.S. Food and Drug Administration
- CFSAN Constituent Update: Taking a Look at the Real-World Impact of the Gluten-Free Labeling Standard
- From: U.S. Food and Drug Administration
- FDA Announces 2017 Public Meetings and Comment Period on Reauthorization of Two Animal Drug User Fee Programs
- From: U.S. Food and Drug Administration
- FDA Issues Final Guidance Clarifying FDA and EPA Jurisdiction over Mosquito-Related Products
- From: 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
- From: U.S. Food and Drug Administration
- Sid Wainer & Son® Initiates Class 1 Recall for Jansal Valley® Dried Chili De Arbol Peppers
- From: U.S. Food and Drug Administration
- Tai Foong Usa Issues Allergy Alert on Undeclared Egg in Product
- From: U.S. Food and Drug Administration
- FDA MedWatch - CORRECTION - Infant Sleep Positioners: FDA Warning - Risk of Suffocation
- From: U.S. Food and Drug Administration
- FDA's Cosmetics News
- From: U.S. Food and Drug Administration
- FDA Approves NORVIR Oral Solution Label
- From: U.S. Food and Drug Administration
- Approved Changes to the DESCOVY Label
- From: U.S. Food and Drug Administration
- FDA MedWatch - Infant Sleep Positioners: FDA Warning - Risk of Suffocation
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: U.S. Food and Drug Administration
- Greencore USA, LLC Recalls Egg Salad Sandwiches
- From: U.S. Food and Drug Administration
- Dean Dairy Conducts Voluntary Recall of Tampico® Brand Tropical Punch
- From: U.S. Food and Drug Administration
- Antiparasitic Resistance in Cattle and Small Ruminants in the U.S.
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: U.S. Food and Drug Administration
- Constituent Update: FDA Proposes to Extend Compliance Dates for Nutrition Facts Label Final Rules
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: U.S. Food and Drug Administration
- FDA Fast Facts: FDA's Support of the Hurricane Relief Effort
- From: U.S. Food and Drug Administration
- FDA improves access to reports of adverse drug reactions
- From: U.S. Food and Drug Administration
- FDA approves new treatment for certain advanced or metastatic breast cancers
- From: U.S. Food and Drug Administration
- OriGen Biomedical Issues Nationwide Recall of OriGen VV28F Reinforced Dual Lumen ECMO Catheters
- From: U.S. Food and Drug Administration
- FDA MedWatch - Endovascular Graft Systems: Letter to Health Care Providers - Type III Endoleaks Associated with Use
- From: U.S. Food and Drug Administration
- King Soopers Recalls Deli Chicken Salad Sandwich (6.8oz) Because of Possible Health Risk
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: U.S. Food and Drug Administration
- 09272017_PR_FDA approves first continuous glucose monitoring system for adults not requiring blood sample calibration
- From: 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
- From: U.S. Food and Drug Administration
- FDA Patient Network Newsletter - Wednesday, September 27, 2017
- From: 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
- From: U.S. Food and Drug Administration
- Federal judge orders Flawless Beauty to stop distributing unapproved drugs, recall certain products
- From: 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
- From: U.S. Food and Drug Administration
- FDA selects participants for new digital health software precertification pilot program
- From: U.S. Food and Drug Administration
- FDA approved changes to the EPIVIR (lamivudine) label
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: 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
- From: 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
- From: U.S. Food and Drug Administration
- Spectranetics Corp. Recalls Bridge Occlusion Balloon Catheter Due to Risk of Blocked Guidewire Lumen Preventing Balloon Utilization
- From: U.S. Food and Drug Administration
- FDA conducts major global operation to protect consumers from potentially dangerous prescription drugs sold online
- From: U.S. Food and Drug Administration
- America New York Ri Wang Food Group Issues Allergy Alert on Seafood Products
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New and Updated)
- From: 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
- From: U.S. Food and Drug Administration
- Criminal and civil actions filed against Aegerion Pharmaceuticals Inc.
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (Updated)
- From: U.S. Food and Drug Administration
- Read about Menopause, Healthy Aging and more
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (Updated)
- From: U.S. Food and Drug Administration
- FDA MedWatch - Ocaliva (obeticholic acid): Drug Safety Communication - Increased Risk of Serious Liver Injury
- From: U.S. Food and Drug Administration
- Nature Supplement Inc. Issues Voluntary Florida Recall
- From: U.S. Food and Drug Administration
- Death Wish Coffee Co. Announces Recall
- From: U.S. Food and Drug Administration
- Gadget Island, Inc. Dba Gear Isle Issues Recall
- From: U.S. Food and Drug Administration
- CFSAN Constituent Update: FDA Releases Training Module for Carriers Subject to the Sanitary Transportation Rule
- From: 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
- From: 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
- From: U.S. Food and Drug Administration
- FDA clears first duodenoscope with disposable distal cap
- From: U.S. Food and Drug Administration
- FDA Drug Shortages (New)
- From: U.S. Food and Drug Administration
- FDA, CDC, and USDA Announce 2017 NARMS Scientific Meeting
- From: U.S. Food and Drug Administration
- Updated MUMS Drug Designations List
- From: U.S. Food and Drug Administration
- Let's Stay Connected!
- 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
- From: U.S. Food and Drug Administration
- FDA Issues Draft Guidance on the Indexing of Legally Marketed Unapproved New Animal Drugs for Minor Species
- From: U.S. Food and Drug Administration
- FDA approves new treatment for adults with relapsed follicular lymphoma
- From: U.S. Food and Drug Administration
- FDA permits marketing of mobile medical application for substance abuse disorder
- From: U.S. Food and Drug Administration
- Food Safety Recalls & Alerts
- What's New at CBER
- From: U.S. Food and Drug Administration
- FDA MedWatch - OriGen VV28F Reinforced Dual Lumen ECMO Catheters: Recall - Potential for Separation of Extension Tube From Hub
- From: U.S. Food and Drug Administration
- OriGen Biomedical Issues Nationwide Recall of OriGen VV28F Reinforced Dual Lumen ECMO Catheters
- From: 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”
- From: U.S. Food and Drug Administration
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Diabetes Infusion Sets by Medtronic: Recall - Vent Membrane May be Susceptible to Being Blocked by Fluid
- Medtronic Announces Voluntary Recall of Diabetes Infusion Sets
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Coborn’s, Inc.’s Issues Recall of American Rye Bread and Caraway Rye Bread Due To Undeclared Allergens
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- September EdNet: The National Food Safety Educator's Network
- CFSAN Constituent Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Update of CVM's What's New - FDA Animal Drug Safety Communication: Micotil 300 User Safety Alert
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Update of CVM's What's New - Taking Care of Your Pets During Hurricanes and Floods
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Update of CVM's What's New - Crops Harvested from Flooded Fields
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- The September 2017 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Baby Organic Liquid Formula by Garden of Life: Recall - Directions For Use May Be Misinterpreted
- Garden of Life LLC Issues Recall of Baby Organic Liquid Formula
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Emergency Preparedness for Medical Devices
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Product Recall By Wegmans Assorted Muffins 4 Pack
- From: U.S. Food & Drug Administration (FDA)
- Product Recall By Wegmans Of Assorted Muffins 4 Pack
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Activase (alteplase) 100mg by Genentech: Recall - Lack of Sterility Assurance
- Genentech Issues Voluntary Nationwide Recall of Three Lots of Activase® (Alteplase)-100 mg Due to Lack of Sterility Assurance of the Sterile Water for Injection
- From: U.S. Food & Drug Administration (FDA)
- Country Fresh Orlando LLC, Recalls Product Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: 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 - Kayexalate (sodium polystyrene sulfonate): Drug Safety Communication - FDA Recommends Separating Dosing
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- CFSAN Constituent Update: FDA Releases Compliance Guide for Small Businesses under FSMA Produce Safety Rule
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Wakefern Food Corp. Voluntarily Recalls ShopRite Semi-Sweet Real Chocolate Chips
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA MedWatch - Unexpired Lots of Oxytocin Compounded with Either Lactated Ringers or Lactated Ringers and Dextrose by PharMEDium - Recall - Sub-Potency
- 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
- From: 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 clears mammography device with option for patient-assisted compression
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Mylotarg for treatment of acute myeloid leukemia
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Federal Veterinarians at Work
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Keytruda (pembrolizumab) in Patients with Multiple Myeloma: FDA Statement - Two Clinical Trials on Hold
- 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.
- From: U.S. Food & Drug Administration (FDA)
- Lucky Mart Inc. Issues Voluntary Nationwide Recall Of Piyanping Anti-Itch Lotion Due to Incorrect Active Ingredient
- From: 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
- From: 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 - Doctor Manzanilla Cough & Cold and Doctor Manzanilla Allergy & Decongestant Relief Syrup: Recall - Potential Contamination with Burkholderia cepacia
- FDA MedWatch - Piyanping Anti-Itch Lotion: Recall - Incorrect Active Ingredient
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Rajbhog Distributors GA Inc. Issues Allergy Alert on Undeclared Almonds in JALEBI
- From: U.S. Food & Drug Administration (FDA)
- Dedinas Franzak Enterprises Issues Allergy Alert On Undeclared Milk In "Butter Flavored Popcorn"
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Forced Air Thermal Regulating Systems: Healthcare Provider Letter - Information About Use
- FDA approval brings first gene therapy to the United States
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update: FDA Releases Sixth Chapter of Draft Guidance for the PC-Human Food Rule
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new antibacterial drug
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first U.S. treatment for Chagas disease
- From: 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
- From: 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
- Update of CVM's What's New - Safety of Food Affected by Hurricanes, Flooding, and Power Outages
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- 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
- Dedinas-Franzak Enterprises Issues Allergy Alert On Undeclared Milk In Big Win Butter Popcorn
- From: U.S. Food & Drug Administration (FDA)
- Cook Medical Issues Recall Correction of Zenith Alpha™ Thoracic Endovascular Graft and Removes Specific Sizes from the Market
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What’s New for Biologics
- From: U.S. Food & Drug Administration (FDA)
- Norovirus & E.coli Food Safety Reminders
- CFSAN Constituent Update: FDA Releases Compliance Guide for Small Businesses under FSMA Intentional Adulteration Rule
- From: U.S. Food & Drug Administration (FDA)
- Recall of Certain Frozen Organic Dark Sweet Pitted Cherry Products Due to Possible Contamination by Listeria Monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Ninjacof and Ninjacof A: Recall - Potential Burkholderia Cepacia Contamination
- Centurion Labs Issues Voluntary Nationwide Recall of Ninjacof (Lot # 200N1601) and Ninjacof A (Lot# 201NA1601) Products Due to Potential <em>Burkholderia Cepacia</em> Contamination
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA Approved Changes to the Odefsey Label
- From: U.S. Food & Drug Administration (FDA)
- Read about Pregnancy Research, Back to School and more
- From: FDA Office of Women's Health
- Update of CVM's What's New - Ornamental Fish Drugs and You
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update: FDA Launches Food Safety Plan Builder to Help Businesses Comply with FSMA Requirements
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Releases Specialized CVM-only Version of eSubmitter Tool
- From: U.S. Food & Drug Administration (FDA)
- Bella Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of All Sterile Drug Products Due to Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sterile Drug Products by Bella Pharmaceuticals: Recall - Lack of Sterility Assurance
- CFSAN Constituent Update - FDA Concludes Major Sampling Study of Sprouts
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- United Trading Inc. Issues Allergy Alert on Undeclared Sulfites in “Gazab Green Raisins (Chinese)”
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA provides new tools for the development and proper evaluation of tests for detecting Zika virus infection
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new treatment for adults with relapsed or refractory acute lymphoblastic leukemia
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Grand BK Corp. Issues Allergy Alert on Undeclared Tree Nuts (Almonds, Walnuts and Cashews) in "California Aloha Mix"
- From: U.S. Food & Drug Administration (FDA)
- Seven Sundays LLC. Recalls Vanilla Cherry Pecan Muesli Because of Possible Health Risk
- From: 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
- Food Safety Recalls & Alerts
- Back to School Food Safety Tips!
- FDA MedWatch - Lorazepam Oral Concentrate, USP 2mg/mL by Amneal Pharmaceuticals: Recall - Misprinted Dosing Droppers
- Food Safety Recalls & Alerts
- Revisions to the GENVOYA Label Approved
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Litehouse Inc. Issues Allergy Alert on Undeclared Egg In Product
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Special Edition EdNet: The National Food Safety Educator's Network
- MADHAVA Natural Sweeteners Issues Allergy Alert on Undeclared Milk in its 13.8 oz. MMM... Chocolate Chip Cookie Mix
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA warns of potential contamination in multiple brands of drugs, dietary supplements
- From: 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.
- From: 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
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Pravastatin Sodium Tablets by International Laboratories: Recall - Mislabeling
- FDA MedWatch -Liquid Products Manufactured by PharmaTech and Distributed by Leader Brand, Major Pharmaceuticals, and Rugby Laboratories: Recall - Possible Product Contamination
- Update of CVM's What's New - Getting Ready for the Next Compliance Dates for FSMA Animal Foods Rule
- From: 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”
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Liquid-filled Intragastric Balloon Systems: Letter to Healthcare Providers - Potential Risks
- FDA MedWatch - Sterile Drug Products from Vital Rx, dba Atlantic Pharmacy and Compounding: FDA Alert - Lack of Sterility Assurance
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Liquid Drug Products Manufactured by PharmaTech and Distributed by Rugby Laboratories and Possibly Other Companies: FDA Advisory - Not to Use
- The Comfy Cow Recalls Pints of Ice Cream Due To Possible E. Coli Contamination and/or High Coliform Counts
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Taylor Farms Retail, Inc. Recalls Coleslaw Kits Due To Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- The August 2017 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- FDA to expand public education campaign to focus on prevention of youth e-cigarette use
- From: U.S. Food & Drug Administration (FDA)
- Freshtex Produce Recalls “Valery” Brand Maradol Papayas Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - FDA Guidances Explain Certain Exemptions from FSMA
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Balguti Kesaria Ayurvedic Medicine: FDA Warning - High Levels Of Lead
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch -Compounded Curcumin Emulsion Product for Injection by ImprimisRx: FDA Investigation - Serious Adverse Events Associated with Use
- Federal judge enters consent decree against outsourcing facility Isomeric Pharmacy Solutions
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- MAVYRET approved to treat HCV
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Mavyret for Hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Diocto Liquid and Diocto Syrup by Rugby Laboratories: Recall - Possible Product Contamination
- Rugby Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup Manufactured By PharmaTech, LLC Due to Possible Product Contamination
- From: 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.”
- From: U.S. Food & Drug Administration (FDA)
- Amrita Health Foods Voluntarily Recalls Protein Bars For Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Fairway ‘‘Like No Other Market’’ ® Recalls Fairway Brand Cookies Blondie Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first treatment for certain types of poor-prognosis acute myeloid leukemia
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Grande Produce Issues Voluntary Recall of Limited Quantity of Papaya “Caribeña” Due to Potential Health Risk (Spanish Version)
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Commonwealth Dairy, LLC Issues Allergy Alert On Undeclared Almond In Aldi Key Lime Crunch Tilts
- From: U.S. Food & Drug Administration (FDA)
- FDA approves treatment for chronic graft versus host disease
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What’s New for Biologics
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Revisions to the Epclusa Label Approved
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new targeted treatment for relapsed or refractory acute myeloid leukemia
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Man of Steel 1 and Man of Steel 2: Recall - Undeclared Drug Ingredient
- FDA MedWatch - 0.9 % Sodium Chloride Injection by ICU Medical: Recall - Presence of Particulate Matter
- August EdNet: The National Food Safety Educator's Network
- Bush Brothers & Company® Recalls Certain Baked Beans in 28 Ounce Cans Due to a Can Seam Issue
- From: U.S. Food & Drug Administration (FDA)
- Vibrant Health Products Issues Allergy Alert On Undeclared Egg In LiveGfree Gluten Free Classic Soft White Hamburger Buns
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: 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
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - Release of Interagency Food Safety Analytics Collaboration (IFSAC) Wrap Up, Action Plan, and Webinar Materials
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cyclobenzaprine HCl and Amantadine HCl by Apace Packaging: Recall - Potential Mislabeling
- Update of CVM's What's New - FDA Informs Veterinarians about Important Labeling Changes to Critical Care Medications for People
- From: U.S. Food & Drug Administration (FDA)
- FDA announces comprehensive regulatory plan to shift trajectory of tobacco-related disease, death
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Grande Produce Issues Voluntary Recall of Limited Quantity of Papaya “Caribeña” Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FW: G-00822-001039
- Hy-Vee, Inc. Issues Allergy Alert on Undeclared Soy in Hy-Vee Brand Pizzas
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA Investigates Multiple Salmonella Outbreak Strains Linked to Papayas
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Sterile Drug Products by Cantrell Drug Company: Recall - Lack of Sterility Assurance
- Cantrell Drug Company Issues Voluntary Nationwide Recall of All Sterile Drug Products Due to Lack of Sterility Assurance
- From: 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
- Update of CVM's What's New - FDA Approves First Medication for Pain Control in a Food-producing Animal
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Enhanced CVM eSubmitter Tool Released
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Releases Revised Guidance about Animal Drug User Fees, Fee Waivers and Reductions
- From: 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
- From: 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
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- The Idaho Foodbank Recalls Coconut Beverage, Broccoli Cheddar Soup, Eggs, and Cheese Product Because Of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Bhu Foods Voluntarily Recalls Protein Bars for Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Summer Food Safety Tips
- Food Safety Recalls & Alerts
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Penumbra 3D Revascularization Device by Penumbra: Class I Recall - Wire Material May Break or Separate During Use
- FDA MedWatch - ED-530XT Duodenoscopes by Fujifilm: Safety Communication - Recall Issued, Updated Design and Labeling
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA clears first neonatal magnetic resonance imaging device
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Garden of Light Inc. Recalls Woodstock Organic Matcha Vanilla Oats Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Vosevi for Hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Vosevi for Hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Texas Legend Foods Issues Allergy Alert on Undeclared Cheese, Milk & Egg in "Silver Star Chipotle Dip"
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Smoke It Low 'N Slow
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- Statement from FDA Commissioner Scott Gottlieb, M.D., on National Academies of Sciences, Engineering, and Medicine report on pain management and prescription opioid abuse
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Read about Pregnancy Research, Caregiving and more
- From: FDA Office of Women's Health
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sten Z and M1 Alpha Capsules by Andropharm: Recall - Contains Derivatives of Anabolic Steroids
- Andropharm Issues Voluntary Nationwide Recall of Sten Z and M1 Alpha Due to Labeling that it Contains Derivatives of Anabolic Steroids
- From: U.S. Food & Drug Administration (FDA)
- Sunneen Health Foods Issues Recall of Parfait Due to Undeclared Allergens
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Coborn's, Inc. Issues Recall of Incorrectly Labeled Gluten Free Chocolate Chip Bars Due To Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Biohealth Nutrition Announces the Recall of Precision Blend Cookies and Cream Product for Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- The July 2017 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new treatment for sickle cell disease
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Atar Extension Cables by Oscor: Recall - Cable Separating from Connector
- Novo Nordisk Recalls Cartridge Holders In Certain Novopen Echo® Insulin Delivery Devices Due to Potential Health Risks
- From: U.S. Food & Drug Administration (FDA)
- Oscor Inc. Issues Nationwide Recall of ATAR Extension Cables
- From: 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 - Ultra-Sten and D-Zine Capsules by Hardcore Formulations: Recall - Contains Anabolic Steroids
- Federal judge enters consent decree against Alabama compounder Medistat
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update - Conversation Series: Expert Insights on Protecting Consumers – Both People and Animals
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- July EdNet: The National Food Safety Educator's Network
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- 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"
- From: U.S. Food & Drug Administration (FDA)
- Stop Food Poisoning from Crashing Your Wedding
- FDA clears expanded use of cooling cap to reduce hair loss during chemotherapy
- From: U.S. Food & Drug Administration (FDA)
- Dierbergs Markets Issues Allergy Alert on Undeclared Fish and Milk in Product
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Federal judge orders New York smoked fish company to stop sales due to food safety violations
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of test to aid in the detection of certain leukemias and lymphomas
- From: U.S. Food & Drug Administration (FDA)
- What's New at CBER Update
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update - FDA Signs MOU with China to Outline Certification Process for Certain Exports
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update - FDA Extends Menu Labeling Compliance Date to 2018
- From: U.S. Food & Drug Administration (FDA)
- FDA unveils plan to eliminate orphan designation backlog
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Potassium Phosphate and Succinylcholine Chloride by PharMEDium Services: Recall - Lack of Sterility Assurance
- PharMEDium Services Issues Voluntary Nationwide Recall of Specific Lots of Potassium Phosphate and Succinylcholine Chloride Due to a Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Publix Recalls Publix Tropical Medley Mix Due to Possible Contamination with Listeria Monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- Publix Recalls Publix Tropical Medley Mix Due to Possible Contamination with Listeria monocytogenes
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA Tackles Drug Competition to Improve Patient Access
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - At FDA, a Long-term Commitment to Engaging Stakeholders
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - ADM Animal Nutrition Recalls Rough-N-Ready Cattle Feed
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Succinylcholine Chloride 20mg/mL 5mL Syringe by Fagron Sterile Services: Recall - Potential Lack Of Sterility Assurance
- Fagron Sterile Services Issues Voluntary Nationwide Recall of Succinylcholine Chloride Due to Potential For Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Teleflex’s (TFX) Vascular Solutions, Inc. Issues Recall of Venture® Catheters
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first subcutaneous C1 Esterase Inhibitor to treat rare genetic disease
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Potassium Phosphate and Succinylcholine by Advanced Pharma: Recall - Potential Lack of Sterility Assurance
- Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Vascular Solutions Inc. Recalls Venture Catheters due to Excess Material that May Split or Separate During Use
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA MedWatch - Venture Catheters by Vascular Solutions: Recall - Excess Material May Split or Separate During Use
- 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
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA and Animal Feed Update
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update - FDA Launches Accredited Third-Party Certification Site
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Batch of Fat Cat Purry-Purry Sauce Hot Sauce Recalled Due to Undeclared Allergens in Per-Peri Pepper Ingredient
- From: U.S. Food & Drug Administration (FDA)
- U.S. Marshals seize adulterated food from a Minnesota warehouse
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Recall Expansion in New Jersey on Fewer than 650 units of Ava’s Brand Organic Roasted Unsalted Cashews and Organic Roasted Unsalted Almonds
- From: U.S. Food & Drug Administration (FDA)
- House of Thaller Recalls Selected Pine Nut Hummus Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- 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.
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Cosmetics News Update
- From: 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
- Datascope Corp/MAQUET Issues Worldwide Voluntary Recall of the System CS100, CS100i and CS300 Intra-Aortic Balloon Pumps for Potential Electrical Test Failure Code
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Chic-A-Peas, LLC Recalls Product Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Update to Voluntary Recall of Eliquis® (apixaban) 5 mg Tablets (#HN0063) - Recall to retail/dispensing level only
- From: U.S. Food & Drug Administration (FDA)
- Vitakraft Sun Seed Issues Voluntary Recall of Certain Rabbit and Macaw Diets Due To Listeria Monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- Alvogen Issues Voluntary Nationwide Recall of Clindamycin Injection Due to a Potential for a Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pet Food Recalls
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA MedWatch - Clindamycin Injection ADD-Vantage Vials by Alvogen: Recall - Lack of Sterility Assurance
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA recently approved changes to the Prezcobix tablet label
- From: U.S. Food & Drug Administration (FDA)
- FDA aproved changes to the Kaletra label
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- NOW Health Group Inc. Expands Voluntary Recall of Ellyndale® Nutty Infusions™ Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Willis Ocean Inc Issues Alert on Uneviscerated Scomber Fish
- From: U.S. Food & Drug Administration (FDA)
- New England Natural Bakers Issues Voluntary Recall Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut <sup>tm</sup> (Sodium Bicarbonate 4% Additive Solution), QUELICIN <sup>tm</sup> (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP Due To a Potential For Lack Of Sterility Assurance
- From: 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
- From: 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
- From: 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
- From: 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
- Food Safety Recalls & Alerts
- FDA MedWatch - Unexpired Nitroglycerin Injection in 5 Percent Dextrose USP by Advanced Pharma in Houston: Recall - Sub Potency
- Food Safety Recalls & Alerts
- FDA MedWatch - Paliperidone Extended-Release Tablets 3mg by Teva Pharmaceuticals: Recall - Dissolution Test Failure
- FDA MedWatch - Frameless Stereotaxic Navigation Systems: FDA Safety Communication - Navigational Accuracy Errors
- Statement from FDA Commissioner Scott Gottlieb, M.D., on the 2016 National Youth Tobacco Survey results
- From: U.S. Food & Drug Administration (FDA)
- Gomacro Recalls Limited Number of Macrobars and Thrive Bars Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Bulletproof 360, Inc. Recalls Collagen Protein Bars and Bites Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Sonar Products ordered to cease operations, Stratus Pharmaceuticals ordered to cease distributing unapproved drugs
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Medical Device Safety and Recalls: Navigational Accuracy Errors Associated with Frameless Stereotaxic Navigation Systems: FDA Safety Communication
- From: U.S. Food & Drug Administration (FDA)
- Read about Summer Safety and more
- From: FDA Office of Women's Health
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Wildway LLC Issues Voluntary Recall of Certain Grain-Free Granola Products
- From: U.S. Food & Drug Administration (FDA)
- Loving Pets Voluntarily Recalls Limited Lot Numbers of Air-Puffed Dog Treats Because of Possible Salmonella Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA MedWatch - Topical Products by Phillips Company: Recall - Due to Concerns of Manufacturing Practices
- Food Safety Recalls & Alerts
- Phillips Company Issues Voluntary Worldwide Recall of All Topical Products Due to Concerns of Manufacturing Practices
- From: U.S. Food & Drug Administration (FDA)
- Heating Things Up
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- 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
- Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg Tablets
- From: U.S. Food & Drug Administration (FDA)
- Giant Eagle Voluntarily Recalls Select Items Due to an Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- CC Kitchens Announces Recall of Limited Number of Salad and Slaw Kits Containing Leafy Greens Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Slade Gorton Co. Inc. Issues Allergy Alert On Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- United Pet Group Voluntary Recalls Multiple Brands of Rawhide Chew Products for Dogs Due to Possible Chemical Contamination
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Club Chef LLC Announces Recall of Limited Number of Snack Kits
- From: U.S. Food & Drug Administration (FDA)
- The June 2017 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- HIV Update: Approval of Generic Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 200 mg/300 mg
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- FDA requests removal of Opana ER for risks related to abuse
- From: U.S. Food & Drug Administration (FDA)
- Happy Sprout Inc. Recalls Soybean Sprouts Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- The FDA warns against using unapproved versions of Juvederm
- From: FDA Office of Women's Health
- Update of CVM's What's New - Animal Drugs at FDA Phase 2 Implementation
- From: U.S. Food & Drug Administration (FDA)
- Norvir (ritonavir) oral powder, 100 mg packet
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- CORRECTION - FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Global Garlic Inc. Recalls "Queso Freso/Whole Milk Cheese" Because of Possible Health Risk
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Medical Device Safety and Recalls: Magellan Diagnostics Inc. Expands Recall for LeadCare Testing Systems Due to Inaccurate Test Results
- From: U.S. Food & Drug Administration (FDA)
- FDA expands use of Sapien 3 artificial heart valve for high-risk patients
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Gilster-Mary Lee Corp. Issues a Recall For Undeclared Egg Noodles in Western Family Onion Soup Mix
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Schnucks Bakery Issues Allergy Alert on Undeclared Walnuts in Cinnamon Pudding Half Cakes and Cake Slices
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals June 2017 Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Hannaford Supermarkets Issues Allergy Alert on Undeclared Milk in Taste of Inspirations Greek Pasta Salad Net. Weight 10 oz. (284g)
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Stay Cool on the Hiking Trail
- 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first generic Strattera for the treatment of ADHD
- From: U.S. Food & Drug Administration (FDA)
- June EdNet: The National Food Safety Educator's Network
- Kroger Issues Allergy Alert on Undeclared Milk in Kroger Yellow Sponge Cake Dessert Cups
- From: U.S. Food & Drug Administration (FDA)
- Kroger Recalls Simple Truth Dry Roasted Macadamia Nuts Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 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
- From: U.S. Food & Drug Administration (FDA)
- Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 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
- From: 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
- From: 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
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - FDA Sampling Finds High Level of Compliance with Gluten-Free Standards
- From: 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
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- 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
- Medical Device Safety and Recalls: Magellan Diagnostics Inc. Recalls LeadCare Plus and Ultra Testing Systems Due to Inaccurate Test Results
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- CFSAN Constituent Update - FSVP: As Compliance Date Nears, Key Facts for Importers
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Caverflo Natural Herbal Coffee: Recall - Presence of Undeclared Active Pharmaceutical Ingredients
- California Sun Dry Foods Announces a Voluntary Recall of Mislabeled California Sun Dry Sun-Dried Tomato Pesto Due to Undeclared Almond and Milk Allergen
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Hail Merry Issues Voluntary Recall Due to Labeling Error
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Al-Er-G Capsules by MusclMasster: Recall - Contains Banned Substance Ephedra
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Special Edition EdNet: The National Food Safety Educator's Network
- Recall of Food Produced at Airway Heights Corrections Center
- From: U.S. Food & Drug Administration (FDA)
- MusclMasster LLC Issues Voluntary Nationwide Recall of Al-Er-G Capsules Because it Contains the Banned Substance Ephedra
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- 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
- From: U.S. Food & Drug Administration (FDA)
- L.A. Lucky Brand Basil Seed 2.1 oz Voluntary Recall Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- 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 approves first cancer treatment for any solid tumor with a specific genetic feature
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
- From: 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
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Tri-Ton by Dynamic Technical Formulations, LLC: Recall - Contains Andarine and Ostarine Drug Ingredients
- FDA MedWatch - V60 Non-invasive Ventilator by Respironics: Class I Recall - Unexpected Device Shut Down
- FDA MedWatch - Gadolinium-based Contrast Agents for Magnetic Resonance Imaging (MRI): Drug Safety Communication - No Harmful Effects Identified With Brain Retention
- Dynamic Technical Formulations, LLC. Issues a Voluntary Nationwide Recall of Tri-Ton Due to the Presence of Andarine and Ostarine
- From: U.S. Food & Drug Administration (FDA)
- BrightFarms Announces Voluntary Regional Recall of Produce Due to Potential Presence of Metal Pieces From Construction
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first drug to specifically treat giant cell arteritis
- From: 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
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- La Nica Products, Inc. Retira Queso Por Posible Riesgo De Salud
- From: U.S. Food & Drug Administration (FDA)
- Wang GlobalNet Issues Allergy Alert Undeclared Eggs, Wheat In “Fish Cake, Fish Ball, And Fish Tofu”
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Henning’s Cheese voluntarily recalls Colby Jack cheese
- From: U.S. Food & Drug Administration (FDA)
- Global Garlic Inc. Recalls Queso Fresco/ Whole Milk Cheese Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA expands approved use of Kalydeco to treat additional mutations of cystic fibrosis
- From: U.S. Food & Drug Administration (FDA)
- La Nica Products, Inc. Recalls Cheese Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA warns Americans about risk of inaccurate results from certain lead tests
- From: FDA Office of Women's Health
- FDA MedWatch - LeadCare Testing Systems (with Blood Obtained from a Vein) by Magellan Diagnostics: FDA Safety Communication - Risk of Inaccurate Results
- FDA warns Americans about risk of inaccurate results from certain lead tests
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: ReFlow Recalls Wingman 35 Crossing Catheters due to Tip Separation
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- FDA MedWatch - Coronary Catheters by Abbott: Recall - Difficulty in Removing Balloon Sheath
- FDA MedWatch - Canagliflozin (Invokana, Invokamet): Drug Safety Communication - Increased Risk of Leg and Foot Amputations
- Italian Gluten Free Food Cl Issues Allergy Alert On Undeclared Egg In “Chef Luca’s Lasagna Al Forno – Baked Cheese Lasagna”
- From: U.S. Food & Drug Administration (FDA)
- Abbott Initiates Voluntarily Recall of Specific Lots of Three Coronary Catheters
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- Green Chile Concepts, Llc Voluntarily Recalls Select Product Codes And Production Dates Of Green Chile Food Company Brand Burrito Products
- From: U.S. Food & Drug Administration (FDA)
- The Horton Fruit Company, Inc. Issues Voluntary Recall of Fresh Spinach Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Read about National Women's Health Week and more
- From: FDA Office of Women's Health
- Allergy Alert Issued by Arabella Station Whole Foods Market for Undeclared Walnuts in Oatmeal Chocolate Chip Cookies
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - CORRECTED LINKS - Looking for More Information on the Foreign Supplier Verification Programs (FSVP) Rule?
- From: U.S. Food & Drug Administration (FDA)
- Food Safety Recalls & Alerts
- Food Safety Recalls & Alerts
- CFSAN Constituent Update - FDA Withdraws Draft Guidance on the Applicability of Color Additive Regulations Authorizing the Use of Certain Fruit Juice and Vegetable Juice
- From: U.S. Food & Drug Administration (FDA)
- FDA authorizes use of new device to treat esophageal birth defect in babies
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Trident Seafoods Corporation Recalls Frozen Multi-Grain Alaskan Cod Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
[Index of Archives]
[CDC News]
[NIH News]
[Epson Inkjet]
[Yosemite]
