FDA News Releases

• Date Index

• FDA approves the first specific treatment for scorpion stings, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare Vital Signs Hygroscopic Condenser Humidifier Passive Humidification Device (HCH): Class I Recall, FDA MedWatch
• CVM Updates - FDA Announces FY 2012 Animal Drug User Fee Rates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arrow International, Inc. Arrow NextStep Antegrade Chronic Hemodialysis Catheter: Class I Recall, FDA MedWatch
• FDA MedWatch - Diflucan (fluconazole): Drug Safety Communication – Long-term, High-dose Use During Pregnancy May Be Associated With Birth Defects, FDA MedWatch
• FDA, international counterparts report progress on drug inspection collaboration, U.S. Food & Drug Administration (FDA)
• FDA reopens comment period on proposed ‘gluten-free’ food labeling rule, U.S. Food & Drug Administration (FDA)
• CVM Updates - The Partnership for Food Protection and FDA Announce Establishment of PETNet, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Voluntary Recall in Oklahoma and Texas of one lot of Purina-Lix 38 Hi-E and RangeLand® 38 Hi-E free-choice supplement tubs for beef cattle, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nestlé Purina Recalls Limited Number of Purina ONE Vibrant Maturity 7+ Dry Cat Food Bags Due to a Potential Health Risk, U.S. Food & Drug Administration (FDA)
• The August 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• RECALL: Cat food (Purina ONE Vibrant Maturity 7+ Dry Cat Food Bags) sold in California, Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, North Dakota, Nebraska, Ohio and Wisconsin, FoodSafety.gov
• Precautionary RECALL: H-E-B Brand cottage cheese, dips, yogurt and sour cream, FoodSafety.gov
• Affordable Care Act Ensures Women Receive Preventive Services at No Additional Cost, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GEM Premier 4000 PAK Cartridges for Use on the GEM Premier 4000 System: Class I Recall - Innaccurate Results, FDA MedWatch
• Ridley Block Operations Announces Voluntary Recall in Oklahoma and Texas, U.S. Food & Drug Administration (FDA)
• Precautionary Recall Issued For H-E-B Brand Dairy Products, U.S. Food & Drug Administration (FDA)
• Nestlé Purina Recalls Limited Number of Purina ONE Vibrant Maturity 7+ Dry Cat Food Bags Due to a Potential Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Fresh Cut Fruit Products Containing Papaya Due To Salmonella, FoodSafety.gov
• RECALL: Beef Due To Potential Animal Drug Contaminant, FoodSafety.gov
• RECALL: Sandwiches, Parfaits, Wraps, Plates, Salads Distributed in Alabama, Georgia, Florida at Starbucks, FoodSafety.gov
• Alert: Three Rivers Brand Golden Raisins Contains Undeclared Sulfites, FoodSafety.gov
• RECALL: Dietary Supplements containing Ephedrine Alkaloids, FoodSafety.gov
• RECALL: Jerky Products Due To Misbranding And An Undeclared Alergen, FoodSafety.gov
• RECALL: Meat Products Produced Without Inspection, FoodSafety.gov
• Flying Food Group Recalls Additional Sandwiches, Parfaits, Wraps, Plates, Salads Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL UPDATE: On Ready-To-Eat Products for Possible Listeria Contamination, FoodSafety.gov
• Enforcement Report for July 27, 2011, U.S. Food & Drug Administration (FDA)
• Intercharm Inc. Issues A Nationwide Voluntary Recall Of Slim Forte Slimming Capsules Lot 20100604 And Lot 20100928, Slim Forte Slimming Coffee Lot 20100903, And Meizitang Botanical Slimming Softgel Exp. 12.23.2011 Weight Loss Capsules Found To Contain Sibutramine, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Silencer S2200 Centrifuge by Global Focus Marketing & Distribution, Ltd.: Class I Recall - Biohazardous Materials May be Released, FDA MedWatch
• CVM Updates - FDA Approves First Drug to Treat Urinary Incontinence in Female Dogs, U.S. Food & Drug Administration (FDA)
• July FDA Basics Webinar: Home Use of Medical Devices, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Methylene Blue: Drug Safety Communication - Serious CNS Reactions Possible When Given to Patients Taking Certain Psychiatric Medications, FDA MedWatch
• FDA MedWatch - Zyvox (linezolid): Drug Safety Communication - Serious CNS Reactions Possible When Given to Patients Taking Certain Psychiatric Medications, FDA MedWatch
• FDA issues draft guidance on device changes that warrant new premarket review, U.S. Food & Drug Administration (FDA)
• Global Focus Marketing & Distribution, Ltd. Recalls The Silencer® S2200 Centrifuge, U.S. Food & Drug Administration (FDA)
• RECALL: All Blondie, Yaya, Mañanita, and Tastylicious Brand Papayas sold before July 23, 2011 Nationwide due to potential Salmonella contamination, FoodSafety.gov
• RECALL: YANT’s Beef Jerky due to Misbranding and Undeclared Allergens, FoodSafety.gov
• RECALL: Chopped beef products “Carne Asada chopped beef and textured wheat protein in red hot sauce” in CA, FoodSafety.gov
• RECALL: “Assoluti Cooked Diced Bacon” bags sold in FL, IL, IN, MI, and OH, FoodSafety.gov
• FDA Center for Drug Evaluation and Research develops strategic science and research agenda, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chantix (varenicline): Label Change, FDA MedWatch
• RECALL: On Uneviscerated Fish in NY (Herring Special Salting), FoodSafety.gov
• Euphoria Fancy Food Inc. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 20, 2011, U.S. Food & Drug Administration (FDA)
• Global Focus Marketing & Distribution, Ltd. Recalls The Silencer® S2200 Centrifuge, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Calcium Gluconate Injection, USP, 10%, 100 mL Pharmacy Bulk Package Due to Particulates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Multaq (dronedarone): Drug Safety Communication - Increased Risk of Death or Serious Cardiovascular Events, FDA MedWatch
  • <Possible follow-ups>
  • FDA MedWatch - Multaq (dronedarone): Drug Safety Communication - Increased Risk of Death or Serious Cardiovascular Events, FDA MedWatch
• CVM Updates - Washington Dairy Farm Permanently Enjoined for Engaging in Unlawful Use of New Animal Drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Oral Osteoporosis Drugs (bisphosphonates): Drug Safety Communication - Potential Increased Risk of Esophageal Cancer, FDA MedWatch
• RECALL: Marinated Beef Products, FoodSafety.gov
• RECALL: Ready-To-Eat Chicken Products, FoodSafety.gov
• Public Comments on New Draft Standards for Data on Race, Ethnicity, Sex, Disability Status, Language, U.S. Food & Drug Administration (FDA)
• FDA approves blood-thinning drug Brilinta to treat acute coronary syndromes, U.S. Food & Drug Administration (FDA)
• Georgia Firm Recalls Ready-To-Eat Chicken Products for Possible Listeria Contamination, FoodSafety.gov
• Arizona Canning Company Issues Allergy Alert On Undeclared Soy Protein In Sun VIsta Brand Red Enchilada Sauce, FoodSafety.gov
  • <Possible follow-ups>
  • Arizona Canning Company Issues Allergy Alert On Undeclared Soy Protein In Sun VIsta Brand Red Enchilada Sauce, U.S. Food & Drug Administration (FDA)
  • Arizona Canning Company Issues Allergy Alert On Undeclared Soy Protein In Sun Vista Brand Red Enchilada Sauce, U.S. Food & Drug Administration (FDA)
• FDA, federal partners develop tools for food-emergency readiness, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Willamette Valley Fruit Co. for undeclared butter in 8” Apple, Cherry & Marionberry Pies, FoodSafety.gov
• FDA approves vaccines for the 2011-2012 influenza season, U.S. Food & Drug Administration (FDA)
• Expanded Recall: Via Xtreme Ultimate Sexual Enhancer Dietary Supplement For Men Recall, U.S. Food & Drug Administration (FDA)
• CardioGen-82 PET Scan: Drug Safety Communication - Increased Radiation Exposure, FDA MedWatch
• CVM Updates - FDA Announces Request for Applications for Evaluation of Salmonella in Symptomatic and Asymptomatic Pets, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update July 14, 2011, U.S. Food & Drug Administration (FDA)
• MedWatch: June 2011 Safety Labeling Changes: 50 products with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 13, 2011, U.S. Food & Drug Administration (FDA)
• Posh Bakery Issues Allergy Alert on Undeclared Eggs in Butter Mini Croissants and Chocolate Mini-Croissants, U.S. Food & Drug Administration (FDA)
• CVM Updates- CVM Expands the Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
• Tamiflu (oseltamivir phosphate) for Oral Suspension: Label Change-New Concentration (6 mg/mL), FDA MedWatch
• ALERGY ALERT: Posh Bakery Issues Allergy Alert on Undeclared Eggs in Butter Mini Croissants and Chocolate Mini-Croissants, FoodSafety.gov
• FDA approves Boostrix to prevent tetanus, diphtheria, and pertussis in older people, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update June 28 - July 1, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nulojix (belatacept): Risk Evaluation and Mitigation Strategy (REMS) - Increased Risk of PTLD and PML, FDA MedWatch
• RECALL: Hawaii Firm Recalls Convenience Meals for Possible Listeria Contamination, FoodSafety.gov
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update July 6, 2011, U.S. Food & Drug Administration (FDA)
• RECALL: South Carolina Firm Recalls Ham Products for Possible Listeria Contamination, FoodSafety.gov
• McNeil Consumer Healthcare Announces Voluntary Recall Of One Product Lot Of TYLENOL ® Extra Strength Caplets 225 Count Distributed In The U.S., U.S. Food & Drug Administration (FDA)
• FDA issues anti-smuggling strategy and draft guidance on new dietary ingredients, U.S. Food & Drug Administration (FDA)
• RECALL: Evergreen Fresh Sprouts Alfalfa Sprouts and Spicy Sprouts Because Of Possible Salmonella Risk, FoodSafety.gov
• CVM Updates - FDA Issues an Announcement of the Availability of Safety and Effectiveness Data to Support a Minor Species New Animal Drug Application, U.S. Food & Drug Administration (FDA)
• FDA approves Arcapta Neohaler to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Valproate Products: Drug Safety Communicaton - Risk of Impaired Cognitive Development in Children Exposed In Utero (During Pregnancy), FDA MedWatch
• FDA MedWatch - Tylenol Extra Strength Caplets, 225 count bottles: Recall - Uncharacteristic Odor, FDA MedWatch
• Check Your Steps: Clean, Separate, Cook, Chill, FoodSafety.gov
• RECALL: Cantaloupes, FoodSafety.gov
• RECALL: Nestlé Purina Dry Cat Food, FoodSafety.gov
• ALLERGY ALERT: Instant Drink Mix Products, FoodSafety.gov
• ALLERGY ALERT: Seafood Salads, FoodSafety.gov
  • <Possible follow-ups>
  • ALLERGY ALERT: Seafood Salads, FoodSafety.gov
• The July 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Risvold’s Salads Inc ISSUES ALLERGY ALERT ON UNDECLARED allergens in Seafood Salad and Seafood Pasta Salad, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nestlé Purina Recalls Limited Number of Dry Cat Food Bags Due to a Potential Health Risk (Shipped Only to Colorado, Idaho and Oregon), U.S. Food & Drug Administration (FDA)
• FDA: Do not eat Evergreen Produce brand alfalfa sprouts or spicy sprouts, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nature Relief Instant Wart and Mole Remover: Recall - Risk of Severe Skin Burns, FDA MedWatch
• FDA MedWatch - Butalbital, Acetaminophen, and Caffeine Tablets (USP 50mg, 325mg, 40mg) and Hydrocodone Bitartrate and Acetaminophen Tablets (USP 7.5mg, 500mg): Recall - Bottle Mislabeled, FDA MedWatch
• CVM Updates - FDA Announces Upcoming NARMS Meeting, U.S. Food & Drug Administration (FDA)
• Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recall of Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP 50mg/325mg/40mg and Four Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg, U.S. Food & Drug Administration (FDA)
• Nature Relief is Conducting a Voluntary Recall of Nature Relief Instant Wart and Mole Remover, U.S. Food & Drug Administration (FDA)
• Eagle Produce, LLC Recalls Cantaloupe Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Endo Pharmaceuticals Issues Voluntary, Nationwide Recall of Two Lots of Endocet® (Oxycodone/Acetaminophen, USP) Tablets, 10 MG / 325 MG, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Erythropoiesis-Stimulating Agents (ESAs) In Chronic Kidney Disease: Drug Safety Communication - Modified Dosing Recommendations, FDA MedWatch
• RECALL: Sausage Products, FoodSafety.gov
• RECALL: Dole & Kroger Italian Blend Salads, FoodSafety.gov
• Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Italian Blend Salads, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - June 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 22, 2011, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT Publix Brand Caesar Salad Dressing, FoodSafety.gov
• RECALL: Frozen Spicy Bean Burgers, FoodSafety.gov
• FDA approves first generic versions of the antibiotic levofloxacin to treat certain infections, U.S. Food & Drug Administration (FDA)
• FDA examines ways to improve consumer understanding of prescription drug ads, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Risperdal (risperidone) and Risperidone: Recall - Uncharacteristic Odor, FDA MedWatch
• Ortho-McNeil-Janssen Pharmaceuticals, Inc. Voluntarily Recalls One Lot of RISPERDAL® Tablets and One Lot of Risperidone Tablets, U.S. Food & Drug Administration (FDA)
• Cinderella Sweets Issues Allergy Alert for Pound Cake Incorrectly Labeled As “Egg Free”, U.S. Food & Drug Administration (FDA)
• FDA unveils new global strategy to help ensure safety and quality of imported products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Boston Scientific Innova Self-Expanding Stent System: Recall - Failure to Deploy, FDA MedWatch
• ALLERGY ALERT: Milk in Chewable Multi Formula, FoodSafety.gov
• ALLERGY ALERT: Pound Cake Incorrectly Labeled As “Egg Free”, FoodSafety.gov
• ALLERGY ALERT: Milk in Burgoo Soup, FoodSafety.gov
• FDA MedWatch - Chantix (varenicline): Label Change - Risk of Certain Cardiovascular Adverse Events, FDA MedWatch
• Enforcement Report for June 15, 2011, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Concentrated Sodium Chloride Injection, USP, 23.4%, 30 mL Single Dose Vial Due to Particulates, U.S. Food & Drug Administration (FDA)
• Staphylococcus Aureus in Queso Fresco Cheese, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Staphylococcus Aureus in Queso Fresco Cheese, FoodSafety.gov
• ATALANTA CORP. Recalls 9 pounds of “Royal Blue Stilton” cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Nulojix for kidney transplant patients, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Indomethacin for Injection: Recall of One Lot - Particulate Matter, FDA MedWatch
• FDA MedWatch - May 2011 Monthly Safety Labeling Changes includes 47 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - Boston Scientific iCross and Atlantis SR Pro 2 Coronary Imaging Catheters: Recall – Catheter Tip Can Break Inside, FDA MedWatch
• FDA MedWatch - Terumo Coronary Ostia Cannula 10, 12, 14 Fr: Recall – Fragments of Adhesive and Plastic in the Cannula Tip May Embolize, FDA MedWatch
• FDA MedWatch - Maquet Datascope Corp. Intra-Aortic Balloon Pumps: Recall – Shuts Off Without Warning, FDA MedWatch
• FDA MedWatch - Risperidone (Risperdal) and Ropinirole (Requip): Medication Errors - Name Confusion, FDA MedWatch
• Inequity to Equity: Promoting Health and Wellness of Women with Disabilities - Call for Proposals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Victoza (liraglutide [rDNA origin]) Injection: Risk of Thyroid C-cell Tumors, Acute Pancreatitis, FDA MedWatch
• Bad Ad Year End Summary, U.S. Food & Drug Administration (FDA)
• FDA approves Potiga to treat seizures in adults, U.S. Food & Drug Administration (FDA)
• FDA approves redesigned labels for some Merck drugs, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications Due by August 5, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 5-alpha reductase inhibitors (5-ARIs): Label Change - Increased Risk of Prostate Cancer, FDA MedWatch
• June 2011 eUpdate - FDA Office of Women's Health, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zocor (simvastatin): Label Change - New Restrictions, Contraindications, and Dose Limitations, FDA MedWatch
• FDA announces new safety recommendations for high-dose simvastatin, U.S. Food & Drug Administration (FDA)
• MGA Recalls Item # 504788BRATZ MAKEUPDesign Sketch Book Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Methyldopate HCL Injection, USP 5 mL Single Dose Vial Due to Glass Particulates, U.S. Food & Drug Administration (FDA)
• Kashi Recalls Select Frozen Pizzas Because They May Contain Plastic Fragments, U.S. Food & Drug Administration (FDA)
• Global Wellness, LLC Conducts a Nationwide Voluntary Recall of VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN Due to Presence of Undeclared Drug, U.S. Food & Drug Administration (FDA)
• FDA: Pfizer will voluntarily suspend sale of animal drug 3-Nitro, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Labeling change for Intron A (Interferon alfa-2b) and PegIntron (Peginterferon alfa-2b), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA: Pfizer will voluntarily suspend sale of animal drug 3-Nitro, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Oridion Medical and Philips Healthcare Microstream CO2 Filterline (FilterLine H Set Infant/Neonate, VitaLine H Set Infant/Neonate: Recall, FDA MedWatch
• HIV/AIDS Update - Commemorating thrity years, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo! Issues Nationwide Recall of Bravo! Pig Ears Dog Chews, U.S. Food & Drug Administration (FDA)
• Simply Thick, LLC Announces The Voluntary Recall Of Products Manufactured By Thermo Pac, LLC At Their Stone Mountain, GA Food Processing Plant, U.S. Food & Drug Administration (FDA)
• Bravo! Issues Nationwide Recall of Bravo! Pig Ears Dog Chews Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Churchill Medical Systems, A Vygon Company, Skin-Prep Wipes used in Convenience Kits, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Aidapak Services Repackaged Pharmaceuticals: Recall - Potential Cross Contamination with Beta Lactam Products, FDA MedWatch
• FDA MedWatch - Thermographic Imaging Systems for Breast Cancer Screening: FDA Safety Communication, FDA MedWatch
• FDA MedWatch - Angiotensin Receptor Blockers (ARBs): Drug Safety Communication - Drug Safety Review Completed, FDA MedWatch
• FDA Safety Communication: Breast Cancer Screening - Thermography is Not an Alternative to Mammography, U.S. Food & Drug Administration (FDA)
• FDA: Treatment with angiotensin receptor blockers for high blood pressure does not increase risk of cancer, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Mountain Trail Mix, FoodSafety.gov
• Update of CVM's What's New - NARMS Retail Meat Annual Report, 2009, U.S. Food & Drug Administration (FDA)
• FDA Enforcement Report Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidance Available - VICH GL36 - Evaluate the Safety of Residues of Veterinary Drugs in Human Food: General Approach to Establish a Microbiological ADI, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Milk And/Or Egg In Onion Rings, FoodSafety.gov
• ALLERGY ALERT: Asian Chicken Noodle Salad, FoodSafety.gov
• RECALL: Primal Pet Foods Feline Chicken & Salmon Formula, FoodSafety.gov
• Birth Control Pills Containing Drospirenone: Possible Increased Risk of Blood Clots, FDA MedWatch
• FDA Drug Safety Communication: Safety Review of possible increased risk of blood clots with birth control pills containing drospirenone, U.S. Food & Drug Administration (FDA)
• The June 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Primal Pet Foods Issues Nationwide Voluntary Recall On Feline Chicken & Salmon Formula, U.S. Food & Drug Administration (FDA)
• FDA approves treatment for Clostridium difficile infection, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA to make enforcement and compliance activities accessible online, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA seeks comment on preventive controls against foodborne illness, U.S. Food & Drug Administration (FDA)
• FDA seeks comment on preventive controls against foodborne illness, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA briefing on boceprevir and telaprevir - follow up, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of tenofovir disoproxil fumarate tablets, 300 mg, U.S. Food & Drug Administration (FDA)
• Globe All Wellness, LLC Issues a Voluntary Recall of Dietary Supplement Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• BCS International Corp. Issues Allergy Alert On Undeclared Peanuts In Dr. Snack Choco Raisin With Sell By Date 03/05/2012, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 25, 2011, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Peanuts In Dr. Snack Choco Raisin, FoodSafety.gov
• Update of CVM's What's New - May 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Beckman Coulter, Inc., Synchron LX Clinical Systems Ion Selective Electrolyte (ISE) Flow Cell: Class I Recall - Incorrect Electrolyte Results, FDA MedWatch
• FDA MedWatch - Pentrexyl Forte Natural: Recall - Misleading Packaging, FDA MedWatch
• Recall of Infant and Neonatal-Sized FilterLine H Set and VitaLine H Set Sampling Lines, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SimplyThick: Public Health Notification - Risk of Life-Threatening Bowel Condition, FDA MedWatch
• FDA: Do not feed SimplyThick to premature infants, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of Edurant (rilpivirine) a new NNRTI) for the treatment of HIV in treatment naive patients, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Food Safety Modernization Act: Focus on Inspections and Compliance Provisions; Public Meeting, U.S. Food & Drug Administration (FDA)
• New FDA Initiative: Enhancing Diversity on FDA Advisory Committees, U.S. Food & Drug Administration (FDA)
• RECALL: Madagascar Bourbon Pure Vanilla Bean Paste, FoodSafety.gov
• Recall: Pig Ears pet treats (PrimeTime and KC Beefhind brands), FoodSafety.gov
• RECALL: Quenby Hall Blue Stilton Cheese, FoodSafety.gov
• RECALL: Pig Ear Pet Treats (Diggers brand), FoodSafety.gov
• BLACKMAN INDUSTRIES, INC. RECALLS PRIMETIME BRAND 2 CT., AND 5 CT. PREMIUM PIG EARS AND KC BEEFHIDE BRAND 20 CT. PREMIUM PIG EARS BECAUSE OF POSSIBLE SALMONELLA HEALTH RISK., U.S. Food & Drug Administration (FDA)
• Schratter Foods Inc RECALLS "Quenby Hall Blue Stilton Cheese" BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• Nielsen-Massey Vanillas, Inc. Issues Voluntary Recall for Specific Lot of Madagascar Bourbon Pure Vanilla Bean Paste, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 18, 2011, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Two Recalls of Pig Ear Products, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Passover Cookies, FoodSafety.gov
• RECALL: Deli Meat Products, FoodSafety.gov
• MedWatch - April 2011 Drug Safety Labeling Changes: 43 products with 22 changes to BW, Contraindications or Warnings, FDA MedWatch
• CORRECTING and REPLACING Mann Packing Reissues and Expands Voluntary Recall of Party Trays and Snacks On The Go Items Containing Grape Tomatoes, U.S. Food & Drug Administration (FDA)
• Phoenix Import & Distribution Announces Recall Of Pentrexyl Forte Natural, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval of VICTRELI (boceprevir) a direct acting antiviral drug to treat hepatitis C virus (HCV), U.S. Food & Drug Administration (FDA)
• FDA warns about counterfeit ExtenZe dietary supplements, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Caution to Pet Owners with the Use of an Unapproved Pet Shampoo Product, U.S. Food & Drug Administration (FDA)
• Bimbo Bakeries USA, Inc. Announces Voluntary Regional Recall Of Entenmann's Bagged Pop'ems Donuts And Bimbo 8 Pack Donitas Donuts Due To Off-Smell And Possible Mold Growth, U.S. Food & Drug Administration (FDA)
• Oberweis Dairy Issues Voluntary Allergen Alert on Undeclared Egg in Brownie Fudge Twirl Ice Cream Quarts, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 11, 2011, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of abacavir sulfate and lamivudine fixed-dose combination tablet for pediatric dosing, U.S. Food & Drug Administration (FDA)
• Mann Packing Reissues And Expands Voluntary Recall Of Party Trays And Snacks On The Go Items Containing Grape Tomatoes, U.S. Food & Drug Administration (FDA)
• Doctor's CarbRite Diet Expands Allergy Alert on Certain Flavored Bars, U.S. Food & Drug Administration (FDA)
• Goodness Gardens, Inc. Recalls Chives Lot # 0201111 Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bottled Water Recall, U.S. Food & Drug Administration (FDA)
• FDA Webinar on Foreign Inspections, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall - Software Defect May Cancel Shock, FDA MedWatch
• Consumers warned to avoid eating oysters from area 1642 in Apalachicola Bay, Florida, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Multi-Mex Distributor Inc. Dietary Supplements: Recall - Product Packaging Mimics OTC Antibiotics, FDA MedWatch
• Multi-Mex Distributor Inc. Announces Recall of Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Produce N.A. Inc. Voluntarily Recalls Grape Tomatoes Grown by Six L's Packing Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Grape Tomatoes Distributed to Albertsons, Raley’s, Safeway, Savemart, Sam’s Club, & Walmart, FoodSafety.gov
• Allergy Alert: Walnuts In GFS Pecan Pieces, FoodSafety.gov
• Allergy Alert: English Muffins and Bread, FoodSafety.gov
• Allergy Alert: J. Gumbo's Chicken Products, FoodSafety.gov
• Allergy Alert: Barbecue Beef, Pork and Chicken Products, FoodSafety.gov
• Northeast Produce Inc. Recalls Grape Tomatoes Due to Salmonella Risk associated with Six L's Packing Company Inc. in Immokalee, FL, U.S. Food & Drug Administration (FDA)
• Ralcorp Frozen Bakery Products Issues Voluntary Allergen Recall of Market Pantry, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Ralcorp Frozen Bakery Products Issues Voluntary Allergen Recall of Market Pantry, FoodSafety.gov
• Dear Abby features Healthy Moms Advice Kit for Women's Health Week, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Needleless Pre-filled Glass Syringes: Drug Safety Communication - Compatibility Problems with Needleless Intravenous Access Systems, FDA MedWatch
• Nut Bar Company Issues Allergy Alert On Undeclared Walnuts In GFS Pecan Pieces, U.S. Food & Drug Administration (FDA)
• Flowers Foods Issues Voluntary Recall on Certain English Muffins and One Bread Item, U.S. Food & Drug Administration (FDA)
• TRI-STATE Baking Company, L.L.C. Issues Allergy Alert On Undeclared Soy Flour, Soy Lecithin, And/Or Milk In Product, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Caffeine & Sodium Benzoate Injection, USP 250 mg/mL, 2 mL Single Dose Vial Due to Visible Particulates, U.S. Food & Drug Administration (FDA)
• Taylor Farms Pacific, Inc. Recalls Grape Tomatoes Due to Salmonella Risk, U.S. Food & Drug Administration (FDA)
• FDA clears first test to quickly diagnose and distinguish MRSA and MSSA, U.S. Food & Drug Administration (FDA)
• FDA expands approved use for carotid stent, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Weck Hem-o-Lok Ligating Clips: Contraindicated for Ligation of Renal Artery During Laparoscopic Living-Donor Nephrectomy, FDA MedWatch
• FDA approves new treatment for rare type of pancreatic cancer, U.S. Food & Drug Administration (FDA)
• RECALL: Pig Ears for Pet Treats (Possible Salmonella), FoodSafety.gov
• ALLERGY ALERT: Portobello Mushroom Flavored Pork Loins Contain Whey (Milk), FoodSafety.gov
• RECALL: Grape Tomatoes, FoodSafety.gov
  • <Possible follow-ups>
  • RECALL: Grape Tomatoes, FoodSafety.gov
• Mastronardi Produce Voluntarily Recalls Grape Tomatoes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Safeway Recalls Kabobs Made with Grape Tomatoes in Several States, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 4, 2011, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New- FDA issues first new rules under Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• FDA issues final guidance for liquid OTC drug products with dispensing devices, U.S. Food & Drug Administration (FDA)
• FDA issues first new rules under Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Keys Manufacturing Company, Inc. Recalls Pig Ears for Pet Treats Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Keys Manufacturing Company, Inc. Recalls Pig Ears for Pet Treats Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• New Features on FDA Office of Women's Health Website, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces the Availability of the NARMS 2008 Executive Report, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Boston Scientific Devices Stolen - Risk of Infection, FDA MedWatch
• FDA, FTC act to remove fraudulent STD products from the market, U.S. Food & Drug Administration (FDA)
• Defibtech Announces a Voluntary Recall of DDU-100 series AEDs, U.S. Food & Drug Administration (FDA)
• Taylor Farms Pacific, Inc. Recalls Grape Tomatoes Due to Salmonella, U.S. Food & Drug Administration (FDA)
• Six L's Voluntarily Recalls Grape Tomatoes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (Warfarin Sodium) Crystalline 5 mg Tablets, Lot Number 9H49374A, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Coumadin (warfarin sodium) Crystalline 5 mg Tablets: Recall - Tablets May Have Higher than Expected Potency, FDA MedWatch
• Update of CVM's What's New - NARMS 2008 Executive Report Now Available, U.S. Food & Drug Administration (FDA)
• The May 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Quinault Tribal Enterprise Recalls All Canned Seafood Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Organic Food Bar, Inc. Expands its Voluntary Recall on Chocolatey Chocolate Chip Bars to Include Additional Products and Lots, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Issue of FDA Veterinarian, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Update to Fuzeon (enfuvirtide) label regarding incidence of bacterial pneumonia, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 27, 2011, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Elise Grace's Dip and Soup Mixes, FoodSafety.gov
• ALLERGY ALERT: Better Batter Mixes, FoodSafety.gov
  • <Possible follow-ups>
  • Allergy Alert: Better Batter Mixes, FoodSafety.gov
• American Regent Initiates Voluntary Nationwide Recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10 mL) 10 mL Single Dose Vial Due to the Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• The Raymond-Hadley Corporation Issues Allergy Alert on Undeclared Milk in Better Batter Brand 20oz. & 2.5lb. Pancake & Biscuit Mix, 18.25oz. Yellow Cake Mix, and 18.25oz. Chocolate Cake Mix, U.S. Food & Drug Administration (FDA)
• Elise Grace's Dry Food Company Issues Nationwide Allergy Alert Because Of Undeclared Allergens In Their Dry Food Products Line, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA Antiviral Advisory Committee April 28, 2011 meeting background materials available: telaprevir for Hepatitis C, U.S. Food & Drug Administration (FDA)
• Woodsmoke Provisions Voluntarily Recalls 160 packages of 4 oz. The Fresh Market Signature Collection Atlantic Smoked Salmon Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• L&M Companies, Inc. Recalls One Lot of Whole Cucumbers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Important Information for Atwater Carey First Aid Kit Consumers Regarding Triad Group's Povidone Iodine Prep Pads, U.S. Food & Drug Administration (FDA)
• Jonathans Sprouts Recalls Alfalfa Sprouts Because of Possible Health Risk Extends Recall of 4/19/11 to Additional Products and Codes ), U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Doctor's CarbRite Chocolate Brownie Diet Bars, FoodSafety.gov
• RECALL: The Fresh Market Signature Collection Atlantic Smoked Salmon, FoodSafety.gov
• ALLERGY ALERT: Carob Brown Rice Crunch Squares & Carob Mint Miniatures, FoodSafety.gov
• RECALL: Whole Cucumbers, FoodSafety.gov
• RECALL: Jonathans Alfalfa Sprouts, FoodSafety.gov
• FDA Hepatitis Update - April 27, 2011 FDA Advisory Committee background materials available: boceprevir for Hep C, U.S. Food & Drug Administration (FDA)
• FDA approves the first vaccine to prevent meningococcal disease in infants and toddlers, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves the first vaccine to prevent meningococcal disease in infants and toddlers, U.S. Food & Drug Administration (FDA)
• Satur Farms, LLC Recalls Satur Farms Cilantro Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Satur Farms, LLC Recalls Satur Farms Cilantro Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Doctor's CarbRite Diet Issues Allergy Alert on Certain Chocolate Brownie Flavored Bars, U.S. Food & Drug Administration (FDA)
• MedWatch - Safety update on Progressive Multifocal Leukoencephalopathy (PML) associated with Tysabri (natalizumab), FDA MedWatch
• Update of CVM's What's New - April 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• RECALL: Summersweet seafood mouses and dips, possible Listeria, FoodSafety.gov
• RECAL: Alfalfa Sprouts, FoodSafety.gov
• Jonathans Sprouts Recalls Alfalfa Sprouts Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA warns companies to stop making MRSA claims for over-the-counter products, U.S. Food & Drug Administration (FDA)
• FDA approves Rituxan to treat two rare disorders, U.S. Food & Drug Administration (FDA)
• B&M, Inc. Conducts Voluntary Nationwide Recall Of 6 Lot Numbers Of Archer Farms Ground Turmeric Due To Excessive Lead Levels., U.S. Food & Drug Administration (FDA)
• Organic Food Bar, Inc. Issues Allergy Alert on Chocolatey Chocolate Chip Raw Organic Food Bars, U.S. Food & Drug Administration (FDA)
• RECALL: Archer Farms Ground Turmeric Sold at Target, FoodSafety.gov
• ALLERGY ALERT: Chocolate Chip Organic Food Bars, FoodSafety.gov
• FDA approves new medical device for form of brain cancer, U.S. Food & Drug Administration (FDA)
• FDA approves Actemra to treat rare form of juvenile arthritis, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 13, 2011, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lansoprazole Delayed-Release Orally Disintegrating Tablets by Teva Pharmaceuticals: Letter to Healthcare Professionals - Clogged, Blocked Oral Syringes and Feeding Tubes, FDA MedWatch
• Ortho-McNeil Neurologics Voluntarily Recalls Two Lots of TOPAMAX®, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Topamax (topiramate): Recall - Musty Odor, FDA MedWatch
• FDA MedWatch - Tumor Necrosis Factor (TNF) blockers, Azathioprine and/or Mercaptopurine: Update on Reports of Hepatosplenic T-Cell Lymphoma in Adolescents and Young Adults, FDA MedWatch
• FDA MedWatch - Penumbra Coil 400 by Penumbra Inc.: Class 1 Recall - Premature Detachment of the Coil, FDA MedWatch
• FDA MedWatch - Axxent FlexiShield Mini by iCAD (formerly Xoft Inc.): Recall - Product May Shed Particles of Tungsten, FDA MedWatch
• FDA approves new treatment for large brain aneurysms, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Shortage Information and Notice of FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• March 2011 Safety Labeling Changes: 55 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Mexicantown Whole Issues Allergy Alert On Undeclared Pecans In Pan Nuez And Undeclared Milk In Magdalena, Pan De Maiz, YoyoPan Nuez, And Tacos De Pan Danes, U.S. Food & Drug Administration (FDA)
• Moog Recalls Curlin Ambulatory Infusion Pump Models 6000 CMS, 6000 CMS IOD, PainSmart, and PainSmart IOD, U.S. Food & Drug Administration (FDA)
• Waco's Bestyett Sandwiches issues a Voluntary Recall of Pimento Cheese Sandwiches and Chicken Salad Sandwiches due to Undeclared EGGS, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Revlimid (lenalidomide): Ongoing Safety Review - increased risk of developing new malignancies, FDA MedWatch
• ALLERGY ALERT: Le Bon Patissier Products, FoodSafety.gov
• ALLERGY ALERT: Chicken of the Sea Chopped Clams May Contain Shrimp, FoodSafety.gov
• RECALL: Spinach, FoodSafety.gov
• FDA clears test for bacteria that can cause serious intestinal disease, U.S. Food & Drug Administration (FDA)
• Tri-Union Seafoods Issues Precautionary, Voluntary Recall Of Limited 6.5-Ounce Chopped Clams, U.S. Food & Drug Administration (FDA)
• FDA approves Horizant to treat restless legs syndrome, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Benzocaine Topical Products: Sprays, Gels and Liquids - Risk of Methemoglobinemia, FDA MedWatch
• Le Bon Patissiere-2, Inc. Announces Voluntary Recall On Select Le Bon Patissiere Products That Contain Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Fresh Express Announces Precautionary Recall of a Limited Number of Cases of 9 oz. Bag Spinach Due to Possible Health Risk from Salmonella, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 6, 2011, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update -, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Hepatitis Update -, U.S. Food & Drug Administration (FDA)
  • FDA Hepatitis Update -, U.S. Food & Drug Administration (FDA)
  • FDA Hepatitis Update -, U.S. Food & Drug Administration (FDA)
• FDA acts to prevent contamination problems with Triad antiseptic products, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for rare form of thyroid cancer, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Listing of Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Veterinary Master Files, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update April 26, 2011, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Yervoy (ipilimumab): Risk Evaluation and Mitigation Strategy (REMS) - Severe Immune-Mediated Adverse Reactions, FDA MedWatch
• FDA Webinar on "Bad Ads" Program on April 28, 2011, U.S. Food & Drug Administration (FDA)
• RECALL: Fitness Labs and Lindberg Protein Supplements, FoodSafety.gov
• RECALL: Smoked Salmon, FoodSafety.gov
  • <Possible follow-ups>
  • RECALL: Smoked Salmon, FoodSafety.gov
• RECALL: Jalapeno Peppers, FoodSafety.gov
• ALLERGY ALERT: Egg in Frozen Chicken Fillets, FoodSafety.gov
• RECALL: Smoked Round Scad Fish (galunggong), FoodSafety.gov
• ALLERGY ALERG: Egg White in Cottage Grove Farmhouse Bakery Breads, FoodSafety.gov
• ALLERGY ALERT: Peanut Oil, Egg, Soy in Sassy Cow Creamery Ice Cream, FoodSafety.gov
• Update of CVM's What's New - FDA launches consumer-friendly Web search for consumers during recalls, U.S. Food & Drug Administration (FDA)
• RECALL: Frankly Fresh Seafood Products, FoodSafety.gov
• RECALL: Sprouts, FoodSafety.gov
• AVNS, Inc. Issues a Voluntary Recall of THE BEST Enhancer, U.S. Food & Drug Administration (FDA)
• FDA launches consumer-friendly Web search for consumers during recalls, U.S. Food & Drug Administration (FDA)
• Cottage Grove Farmhouse Bakery Issues Allergy Alert On Undeclared Pasteurized Egg White In Breads, U.S. Food & Drug Administration (FDA)
• Centurion Medical Products Initiates Voluntary Recall of Customized Convenience Kits (including select Central Venous Catheter, PICC Insertion, and VAD Trays) that contain American Regent's Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials, U.S. Food & Drug Administration (FDA)
• The April 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Arko Foods International Recalls Angelina Brand Smoked Roundscad Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Arko Foods International Recalls Angelina Brand Smoked Roundscad Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Louie Foods International Voluntarily Recalls Certain Sprouts, U.S. Food & Drug Administration (FDA)
• Frankly Fresh Inc. Voluntarily Recalls Seafood Salad Products Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA proposes draft menu and vending machine labeling requirements, invites public to comment on proposals, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Labeling changes to Tyzeka (telbivudine) 600 mg tablets and oral solution 100 mg/5 mL reflect risk of resistance-associated substitutions, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heartstring II Proximal Seal System (HS-1045) by Maquet Cardiovascular, LLC: Recall - Insufficient Adhesive, FDA MedWatch
• FDA MedWatch - Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F by Millar Instruments Inc.: Class 1 Recall, FDA MedWatch
• THE SMOKEHOUSE LLC RECALLS ONE BATCH OF PORTIER FINE FOODS NORWEGIAN SMOKED SALMON BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Meds IV Pharmacy, IV Compounded Products Recall: Outbreak of Serratia Marcescens Bacteremia in Alabama Hospitals, FDA MedWatch
• CDC And ADPH Investigate Outbreak At Alabama Hospitals; Products Recalled, U.S. Food & Drug Administration (FDA)
• New Cosmetics Consumer Update and Video, U.S. Food & Drug Administration (FDA)
• Nutrition Express Voluntarily Recalls Protein Supplements Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Trader Joe's Pizza Al Pollo Asado, FoodSafety.gov
• FDA MedWatch - Pradaxa (dabigatran etexilate mesylate) Capsules: Special Storage and Handling Requirements, FDA MedWatch
• HIV/AIDS Update - Tentative approval of emtricitabine capsules, 200 mg, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces the Approval of Iron Dextran for Baby Pigs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - X-Hero and Male Enhancer: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - Roche ACCU-CHEK FlexLink Plus Infusion Set: Class I Recall - Potential for Under-Delivery of Insulin, FDA MedWatch
• Recall of Arnica Flower And Stem Arnica Due To Inaccurate Usage Information On Product Label, U.S. Food & Drug Administration (FDA)
• USA Far Ocean Group Inc. Issues Voluntary Nationwide Recall of X-Hero and Male Enhancer, Products Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Soladek Vitamin Solution: Unapproved Product May Contain Dangerously High Levels of Vitamins A and D, FDA MedWatch
• HIV/AIDS Update - Approval of VIRAMUNE XR (nevirapine) 400 mg extended release tablet, U.S. Food & Drug Administration (FDA)
• RECALL: Bubble Gum with Elevated Levels of Lead, FoodSafety.gov
• ALLERGY ALERT: Egg in Mai's Bakery Hopia Mongo and Moon Cake Products, FoodSafety.gov
• FDA MedWatch - Citalopram And Finasteride by Greenstone: Recall - Possible Mislabeling, FDA MedWatch
• FDA MedWatch - Irinotecan Hydrochloride Injection: Recall - Fungal Microbial Contaminant, FDA MedWatch
• Candy Dynamics Recalls Toxic Waste® Short Circuits[TM] Bubble Gum Net wt. 3.2 oz. (90g) Package --- Lot # 15070SC12, U.S. Food & Drug Administration (FDA)
• APP Pharmaceuticals Issues A Nationwide Voluntary Recall Of Irinotecan Hydrochloride Injection, U.S. Food & Drug Administration (FDA)
• Greenstone Announces Voluntary Nationwide Recall Of Citalopram And Finasteride Due to Possible Mislabeling, U.S. Food & Drug Administration (FDA)
• Mai's Bakery Issues Allergy Alert For Undeclared Eggs in Their Packages of "Hopia Mongo" and "Moon Cake" Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FR Notice; Extension of Comment Period for The National Antimicrobial Resistance Monitoring System Strategic Plan 2011-2015, U.S. Food & Drug Administration (FDA)
• RECALLS: Serrano Peppers, Protein Supplements, Smoked Ham and Bacon Products, Pickled Beets, Bologna, Cantaloupes, FoodSafety.gov
• ALLERGY ALERTS: Kashi Southwest Style Chicken Products, Wheat Bread, FoodSafety.gov
• FDA approves Zostavax vaccine to prevent shingles in individuals 50 to 59 years of age, U.S. Food & Drug Administration (FDA)
• Unified Grocers Issues Allergy Alert on Undeclared Milk in Cottage Hearth Stone Ground Wheat Bread (24 oz) and 7 Select 100% Whole Wheat Bread (24 oz), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA and the Assoc. of American Feed Control Officials collaborate on the development of Animal Feed Regulatory Program Standards, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - March 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• USA Far Ocean Group, Inc. Issues Voluntary Nationwide Recall of U-Prosta, a Product Marketed As a Dietary Supplement That Contains Undeclared Terazosin Hydrochloride, U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Poduce Voluntairly Recalls Cantalopes Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 23, 2011, U.S. Food & Drug Administration (FDA)
• Millar Instruments, Inc. Issues a Recall of Millar Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Draft Guidance for Industry: Testing for Salmonella Species in Human Foods and Direct-Human-Contact Animal Foods, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - H&P Industries Povidine Iodine Prep Pads: Recall - Potential Microbial Contamination, FDA MedWatch
• Lilly Announces Important Action Regarding Recall of Alcohol Prep Pads Made by Triad Group Included in Forteo Starter Kits, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Single Dose Vials; 5 mL and 30 mL Multiple Dose Vials, U.S. Food & Drug Administration (FDA)
• H&P Industries, Inc. Issues a Voluntary Nationwide Recall of All Lots of Povidine Iodine Prep Pads Due to Potential Microbial Contamination, U.S. Food & Drug Administration (FDA)
• World Variety Produce, Inc. Recalls Serrano Peppers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - American Regent Injectable Products: Recall - Visible Particulates in Products (UPDATE), FDA MedWatch
• FDA MedWatch - Gen-Probe Inc., AccuProbe Group B Streptococcus Culture Identification Test, AccuProbe Mycobacterium Tuberculosis Complex Culture Identification Test and, AccuProbe Mycobacterium Avium Complex Culture Identification Test: Class I Recall, FDA MedWatch
• New FDA Basics Question: Is the U.S. really slower than Europe in approving new drugs?, U.S. Food & Drug Administration (FDA)
• New FDA Basics Question: Is it true FDA is approving fewer new drugs lately?, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 16, 2011, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Nationwide Recall of Concentrated Sodium Chloride Injection, USP, 23.4% 30 mL Single Dose Vials and 100 mL Pharmacy Bulk Packs, U.S. Food & Drug Administration (FDA)
• RECALL: Herring and Sprats, FoodSafety.gov
• Update of CVM's What's New - Veterinary Laboratory Response Network, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated GRAS Notices Inventory and Updated Listing of Approved Medicated Feed Mill Licenses, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA Advisory Committee meeting to consider boceprevir and telaprevir, April 27 and April 28, 2011, U.S. Food & Drug Administration (FDA)
• February 2011 Safety Labeling Changes: 53 Medical Product Labels with changes to Prescribing Information, FDA MedWatch
• RECALL: Lean Cuisine Spaghetti with Meatballs, FoodSafety.gov
• RECALL: Organic Garbanzo Beans, FoodSafety.gov
• RECALL: Frozen pb jamwich from Giant-Carlisle Stores, FoodSafety.gov
• PIERRE FOODS Voluntarily Recalls 320 Cases Of Pierre TM pb jamwich, LOT 0068035 From Giant-Carlisle Stores IN MD, PA, VA AND WV, U.S. Food & Drug Administration (FDA)
• Faribault Foods Announces Voluntary Recall of Field Day Organic Garbanzo Beans Due to Mislabeling and Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Is there lead in lipstick?, U.S. Food & Drug Administration (FDA)
• Does FDA approve the color additives used in cosmetics? If so, how does FDA determine their safety?, U.S. Food & Drug Administration (FDA)
• Are henna tattoos safe?, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Beef Sticks, FoodSafety.gov
• ALLERGY ALERT: Turkey Stick Products, FoodSafety.gov
• RECALL: Chocolate Milk, FoodSafety.gov
• RECALL: Coconut Water, FoodSafety.gov
• ONE World Enterprises Recalls O.N.E. Coconut Water Due To Mold, U.S. Food & Drug Administration (FDA)
• Oak Farms Dairy in Waco Conducts Voluntary Limited Recall of Half Gallon Plastic Bottles of Whole Chocolate Milk, Half Pint Paper Cartons of Whole Chocolate Milk, and Half Pint Paper Cartons of 1% Chocolate Milk Due to Presence of Alkaline Phosphatase in Samples, U.S. Food & Drug Administration (FDA)
• Vitalabs, Inc. Issues Voluntary Recall for Specific Lots of Whey Protein Isolate, U.S. Food & Drug Administration (FDA)
• RECALL: Pig Ear Dog Chews, FoodSafety.gov
• RECALLS: Organic Herbal Tea, FoodSafety.gov
• RECALL: Bologna, FoodSafety.gov
• CVM Updates - FDA Releases Electronic Submission Tool, eSubmitter, for Use by the Animal Health Industry, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA to Convene Public Hearing on Ensuring the Safety of Imported Foods and Animal Feed, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Draft Guidance Available, U.S. Food & Drug Administration (FDA)
• FDA, Justice Department take action against McNeil-PPC Inc., U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Advises Veterinarians of Recent Recall of Human Drug, Phenobarbitol, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 9, 2011, U.S. Food & Drug Administration (FDA)
• FDA approves Benlysta to treat lupus, U.S. Food & Drug Administration (FDA)
• FDA approves Benlysta to treat lupus--First new lupus drug approved in 56 years, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval for Lamivudine and Tenofovir DF Fixed Dose Combination Tablets, 300 mg/300 mg, U.S. Food & Drug Administration (FDA)
• RECALL: Ground Beef, FoodSafety.gov
• Update of CVM's What's New - Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• REMEDYTEAS Voluntarily Recalls Peppermint Organic Herbal Tea And Organic Herbal Tea Blend Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Jones Natural Chews Co Recalls Pig Ear Dog Chews Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Webinar on Tattoos and Permanent Makeup, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Kaletra (lopinavir/ritonavir): Label Change - Serious Health Problems in Premature Babies, FDA MedWatch
• McCormick & Company Recalls Golden Dipt® Tempura Seafood Batter Mix Due To Unlabeled Milk Ingredient, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Golden Dipt Tempura Seafood Batter Mix, FoodSafety.gov
• Unilever Announces Recall of Skippy® Reduced Fat Peanut Butter Spread Due to Possible Health Risk Limited Recall of 6 Best-If-Used-By Dates, U.S. Food & Drug Administration (FDA)
• DeFranco and Sons Recall Bulk and Consumer-packaged In-shell, Hazelnut and Mixed Nut Products Containing Hazelnuts, U.S. Food & Drug Administration (FDA)
• FDA: E. coli O157:H7 cases linked to hazelnuts, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The due date for applying to CVM's 2011 Summer Intern Program "Windows to Regulatory Research" has been extended to March 18, 2011, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval for abacavir sulfate scored tablets for oral suspension, 60 mg, U.S. Food & Drug Administration (FDA)
• FDA modifies boxed warning for pulmonary arterial hypertension drug Letairis, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Topamax (topiramate): Label Change - Risk For Development of Cleft Lip and/or Cleft Palate in Newborns, FDA MedWatch
• FDA: Risk of oral birth defects in children born to mothers taking topiramate, U.S. Food & Drug Administration (FDA)
• Food Co. Recalls Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA expands use of banding system for weight loss, U.S. Food & Drug Administration (FDA)
• Garden of Life, LLC. Issues a Voluntary Recall of Vitamin Code Raw Vitamin C Dietary Supplement. Recall is Limited to Raw Vitamin C Only. No Other Garden of Life Products are Involved., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Davol XenMatrix Surgical Graft: Class I Recall - Elevated Endotoxin Levels, FDA MedWatch
• FDA MedWatch - Cook Inc., Single, Double, Triple and Five-Lumen Central Venous Catheter Trays, Single and Double Lumen PICC Peripheral Inserted Central Venous Catheter Trays Recall, FDA MedWatch
• Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Current Animal Food GRAS Notices Inventory, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 2, 2011, U.S. Food & Drug Administration (FDA)
• FDA prompts removal of unapproved drugs from market, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unapproved Cough, Cold, Allergy Products: FDA Prompts Removal From Market, FDA MedWatch
• FDA MedWatch - Proton Pump Inhibitor drugs (PPIs): Drug Safety Communication - Low Magnesium Levels Can Be Associated With Long-Term Use, FDA MedWatch
• Update of CVM's What's New - The Story of the Center for Veterinary Medicine (video), U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Safety Review update of Abacavir: no statistically significant association seen between myocardial infarction and ABC, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Wellpet LLC Voluntarily Recalls Certain Lots Of Canned Cat Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Abacavir - Ongoing Safety Review: Possible Increased Risk of Heart Attack, FDA MedWatch
• FDA approves new drug to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
• E&J Brandy Announces A Nationwide Recall Of Stainless Steel Flasks Due To Possible Lead Risk, U.S. Food & Drug Administration (FDA)
• W H & GROUP, LLC. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• The March 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves Edarbi to treat high blood pressure, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Negative Pressure Wound Therapy (NPWT) systems UPDATE, FDA MedWatch
• ALLERGY ALERT: Maya Dry Fruit Kachori contains peanuts, FoodSafety.gov
• ALLERGY ALERT: Nibble with Gibble's and Kay & Ray's Chips May Contain Soy, FoodSafety.gov
• RECALL: Pacific American Fish Roe Capelin, Risk of Botulism, FoodSafety.gov
• ALLERGY ALERT: Haddon House Asian Gourmet Cheese Rice Crackers, FoodSafety.gov
• Arkansas Firm Recalls Various Meat and Poultry Products Produced Without Inspection, FoodSafety.gov
• FDA: Advanced genomic test helps trace sources of foodborne illness outbreak, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Kaletra (lopinavir/ritonavir) Oral Solution label changes related to toxicity in preterm neonates, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Label change for Viracept (nelfinavir): drug-drug interaction information with warfarin, U.S. Food & Drug Administration (FDA)
• Urgent Recall on Asian Gourmet Cheese Rice Crackers Which May Contain Undeclared Milk and Undeclared Food Coloring Additives., U.S. Food & Drug Administration (FDA)
• Svelte 30 Nutritional Consultants Issues a Voluntary Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• FDA and Georgetown University Medical Center announce partnership, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of zidovudine water-disperable tablets, 100 mg for pediatrics/adults unable to swallow tablets, U.S. Food & Drug Administration (FDA)
• Roche Insulin Delivery Systems announces recall of ACCU-CHEK® FlexLink Plus infusion sets, U.S. Food & Drug Administration (FDA)
• Consumer Alert: Undeclared Peanuts In Dry Fruit "Kachori", U.S. Food & Drug Administration (FDA)
• FDA: U.S. Marshals seize food products at Tennessee company, U.S. Food & Drug Administration (FDA)
• Martin's Famous Pastry Shoppe, Inc. Issues Allergy Alert On Undeclared Soy Protein In Certain "Nibble With Gibble's" And Kay And Ray's Branded Products, U.S. Food & Drug Administration (FDA)
• Pacific American Fish Co. Recall Shishamo Roe Capelin 4L Due To Potential of C. Botulinum, U.S. Food & Drug Administration (FDA)
• Advanced genomic test helps trace sources of foodborne illness outbreak, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 23, 2011, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2011 Safety Labeling Changes; 43 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - Extenze Tablets: Recall, FDA MedWatch
• BIOTAB NUTRACEUTICALS, INC. Issues a Voluntary Recall of Specific Lots of the Nutritional Supplement EXTENZE (Men's Regular), U.S. Food & Drug Administration (FDA)
• FDA permits marketing of first test for most common cause of gastroenteritis outbreaks, U.S. Food & Drug Administration (FDA)
• Natural Choice Distribution Company Inc. Voluntarily Recalls Certain Lots Of Fare And Square Sandwiches, Superfresh Sandwiches, And Real Wraps Burritos Due To The Presence Of Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• PHOTO - Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• Upsher-Smith Laboratories Announces Expansion of Voluntary Nationwide Recall. Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven® and Oxybutynin, U.S. Food & Drug Administration (FDA)
• Hua Shing International Trading Corp Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Antipsychotic Drugs: Class Labeling Change - Treatment During Pregnancy and Potential Risk to Newborns, FDA MedWatch
• Safety is NO Accident...National Public Health Week April 4-10, 2011, U.S. Food & Drug Administration (FDA)
• FDA approves product to prevent bleeding in people with rare genetic defect, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Notice of Extension of Comment Period; Unapproved Animal Drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Warfarin Sodium Tablets (Jantoven), 3mg: Recall - Mislabeled Bottles Containing Higher Dosage, FDA MedWatch
• FDA warns against certain uses of asthma drug terbutaline for preterm labor, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Terbutaline: Label Change - Warnings Against Use for Treatment of Preterm Labor, FDA MedWatch
• HIV/AIDS Update - Tentative approval of abacavir sulfate Oral Solution, 20 mg/mL, U.S. Food & Drug Administration (FDA)
• Upsher-Smith Laboratories Announces The Voluntary Nationwide Recall Of Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 16, 2011, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize Auralgan Otic Solution, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic SynchroMed II and SynchroMed EL Implantable Infusion Pump and Refill Kits: Class 1 Recall, FDA MedWatch
• Prime Choice Foods Corporation Voluntarily Recalls Certain Lots Of Garden Of Eatin'® Multi Grain Tortilla Chips Due To The Presence Of Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Triad Sterile Lubricating Jelly: Recall - Product May Not Be Sterile, FDA MedWatch
• FDA seeks to invest in foodborne illness prevention, medical product safety and countermeasures, U.S. Food & Drug Administration (FDA)
• FDA finalizes regulation for certain software, hardware used with medical devices, U.S. Food & Drug Administration (FDA)
• January, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT EXPANDED: f'realStrawberry Banana Smoothies -- May Contain Peanuts, FoodSafety.gov
• f'real® foods Expands Voluntary Recall Of Strawberry Banana Smoothies Due To Potential Peanut Content, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Barbecue Pork Sold in AL, GA, TN, MS, may contain dairy (whey), FoodSafety.gov
• ALLERGY ALERT: Essentials, RightFood, other BioSan dietary supplements, may contain soy, FoodSafety.gov
• ALLERGY ALERT: H-E-B Frozen Breaded Okra Sold in Texas, may contain dairy (whey), FoodSafety.gov
• RECALL: Smoked Salmon sold at The Fresh Market, possible Listeria, FoodSafety.gov
• RECALL: Ground Beef Products (Possible E. Coli Contamination), FoodSafety.gov
• ALLERGY ALERT: f'real® Strawberry Banana Smoothies may contain peanuts, FoodSafety.gov
• ALLERGY ALERT: Frozen Yellow Fin Tuna, FoodSafety.gov
• FDA approves first 3-D mammography imaging system, U.S. Food & Drug Administration (FDA)
• f'real® foods Issues Voluntary Recall of Strawberry Banana Smoothies Due to Potential Peanut Content, U.S. Food & Drug Administration (FDA)
• FDA clears test to help patients with kidney transplants, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - February 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• St James Smokehouse, Inc, Announces Voluntary Recall of Scotch Reserve Whiskey & Honey Smoked Salmon 4oz Retail Packs Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Neuro Resource Group, Inc. Informs Customers of Important Information about Triad Group's Alcohol Prep Pads, U.S. Food & Drug Administration (FDA)
• FDA Webinar on Safety of the Blood Supply, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 9, 2011, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arstasis One Access System: Class I Recall - Components May Fracture and/or Separate, FDA MedWatch
• Are all personal care products regulated as cosmetics?, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Are all personal care products regulated as cosmetics?, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Letter to Veterinarians and Pharmacy Professionals re: SucroMate Equine (deslorelin acetate), U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Important information about alcohol prep pads packaged with Pegasys and certain other injection products, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Important information about alcohol prep pads packaged with Fuzeon and certain other injection products, U.S. Food & Drug Administration (FDA)
• Pandemic Influenza Evaluation and Capacity Review Tools, U.S. Dept. of Health & Human Services
• How do the activities of the USDA FSIS differ from the activities of the FDA Center for Food Safety and Applied Nutrition?, U.S. Food & Drug Administration (FDA)
• FDA launches Medical Device Innovation Initiative, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hydrocodone Bitartrate And Acetaminophen Tablets, Phenobarbital Tablets by Qualitest: Recall - Incorrect Package Labeling, FDA MedWatch
• FDA orders postmarket surveillance of certain TMJ implants, U.S. Food & Drug Administration (FDA)
• Rouses Markets Voluntarily Recalls Frozen Yellow Fin Tuna Steaks Due To Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Watson Announces Important Action Related to Nationwide Recall of Triad Alcohol Prep Products Included in Products, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Potassium Phosphates Injection, USP 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium 5 mL Single Dose Vial, Lot# 0048 Due to Translucent Visible Particles, U.S. Food & Drug Administration (FDA)
• Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall Of Hydrocodone Bitartrate And Acetaminophen Tablets, USP 10 MG / 500 MG, NDC 0603-3888-20, 60 Count, Lot Numbers T150G10B, T120J10E And T023M10A And Phenobarbital Tablets, USP 32.4 MG, NDC 0603-5166-32, 1000 Count, Lot Numbers T150G10B, T, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - American Regent Injectable Products: Recall - Visible Particulates in Products, FDA MedWatch
• HIV/AIDS Update - Reyataz (atazanavir) label revised, adding dosing recommendations for pregnancy and postpartum period, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Merit Prelude Short Sheath Catheter Introducer: Class I Recall - Tip May Detach During Use, FDA MedWatch
• CVM Updates - FDA Announces Upcoming Shortage of Vetsulin for Dogs and Cats in the Critical Need Program, U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health eUpdate, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Apple Chipotle Salsa, Maple BBQ Grilling Sauce, & Pumpkin Chipotle Roasting Sauce (contain wheat), FoodSafety.gov
• ALLERGY ALERT: Mooney's Kentucky Bourbon Cheese & Valumarket's Beer Cheese Spread (contains soy and fish), FoodSafety.gov
• ALLERGY ALERT: Mariegold Baking White Bread and Vallarta Premium White Bread (contain milk), FoodSafety.gov
• ALLERGY ALERT: Caesar Dressing (contains eggs), FoodSafety.gov
• American Spoon Foods brand Apple Chipotle Salsa, Maple BBQ Grilling Sauce, and Pumpkin Chipotle Roasting Sauce may contain undeclared wheat flour and may put certain consumers at risk for wheat or gluten sensitivities or allergies., U.S. Food & Drug Administration (FDA)
• FDA clears first diagnostic radiology application for mobile devices, U.S. Food & Drug Administration (FDA)
• Shaping Beauty, Inc. Issues a Voluntary Nationwide Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Sodium Thiosulfate Injection, USP 10% (100 mg/mL) 10 mL Single Dose Vials Lot# 0056 Due to Translucent Visible Particles, U.S. Food & Drug Administration (FDA)
• FDA approves drug to reduce risk of preterm birth in at-risk pregnant women, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - UPDATE: Avandia (rosiglitazone): Information on cardiovascular risks (including heart attack) added to labeling and Medication Guide, FDA MedWatch
• Updated: Undeclared Soy And Anchovy Puree In "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread", U.S. Food & Drug Administration (FDA)
• Godi International, Corp. Issues a Voluntary Nationwide and International Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement., U.S. Food & Drug Administration (FDA)
• Unified Grocers Issues Allergy Alert on Undeclared Milk in Mariegold Baking White Bread (24 oz) and Vallarta Premium White Bread (24 oz), U.S. Food & Drug Administration (FDA)
• Tomaso's Issues Allergy Alert On Undeclared Eggs In Caesar Dressing, U.S. Food & Drug Administration (FDA)
• FDA reminds health care professionals about safe use of non-sterile alcohol prep pads, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Guidance - Target Animal Safety & Effectiveness Protocol Development & Submission, U.S. Food & Drug Administration (FDA)
• Magic Valley Fresh Frozen, Inc. Foods Issues Allergy Alert On Undeclared Milk In Breaded Okra, U.S. Food & Drug Administration (FDA)
• Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group's Alcohol Prep Products, U.S. Food & Drug Administration (FDA)
• Sabor Farms Recalls Four Brands Of Cilantro Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Fresh Cilantro, FoodSafety.gov
• FDA MedWatch - B. Braun Outlook 400ES Safety Infusion System, Model Number 621-400ES: Class I Recall - Hardware May Become Unresponsive, FDA MedWatch
• RECALL: Horse Feed Distributed in California, Nevada, and Oregon, FoodSafety.gov
• RECALL: Jr. Texas JR Taffy pet treat, possible Salmonella, FoodSafety.gov
• ALLERGY ALERTS: Ice Cream, Cheese, Veal Ravioli, FoodSafety.gov
• The February 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - January 2011 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - two recalls - Family Farm Complete Horse 10 horse feed and Jr. Texas Taffy pet treat, U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Ice Cream Containing Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• MERRICK PET CARE RECALLS JR TEXAS TAFFY PET TREAT (ITEM # 27077, ALL LOTS UP TO AND INCLUDING 10364) BECAUSE OF POSSIBLE SALMONELLA HEALTH RISK, U.S. Food & Drug Administration (FDA)
• Feed Manufacturer Issues Limited Voluntary Recall of a Horse Feed Product Distributed in California, Nevada, and Oregon, U.S. Food & Drug Administration (FDA)
• Undeclared Soy in "Mooney's Kentucky Bourbon Cheese" and "Valumarket's Beer Cheese Spread", U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Keebler Fudge Shoppe Jumbo Fudge Sticks sold at convenience stores, FoodSafety.gov
• RECALL: All Toxic Waste brand Nuclear Sludge Products, FoodSafety.gov
• KEEBLER ISSUES ALLERGY ALERT ON MISLABELED 8-COUNT CARTONS OF FUDGE SHOPPE® JUMBO FUDGE STICKS SOLD AT CONVENIENCE STORES, U.S. Food & Drug Administration (FDA)
• Candy Dynamics Expands Recall to all Toxic Waste® brand Nuclear Sludge® Products all flavors and all sizes, U.S. Food & Drug Administration (FDA)
• PEEKAY INTERNATIONAL INC. ISSUES ALLERGY ALERT ON UNDECLARED SULFITES IN SWAN GOLDEN RAISINS, U.S. Food & Drug Administration (FDA)
• Important information for ARIXTRA® Starter Kit patients regarding Triad Group's alcohol prep products, U.S. Food & Drug Administration (FDA)
• Fourth FDA orphan drug designation workshop scheduled for Feb. 28 - March 1, 2011, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERTS: Calamari, Corn Pops, Shrimp, Potato Chips, FoodSafety.gov
• RECALL: Wide Variety of Salad Greens, Including Organic, Sold on the East Coast, FoodSafety.gov
• State Garden, Inc. Announces Voluntary Recall Of Certain Salad Mixes Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pfizer Inc. And Progenics Alert Physicians And Patients To Information Related To Triad Group Alcohol Prep Products Included In U.S. RELISTOR Kit Packaging, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Breast Implants: FDA Review Indicates Possible Association With A Rare Cancer, FDA MedWatch
• FDA review indicates possible association between breast implants and a rare cancer, U.S. Food & Drug Administration (FDA)
• RECALL: Two of Ian's brand Frozen Entrees, FoodSafety.gov
• Ian's Voluntarily Recalls Two Products Due To Risk Of Contamination By Listeria Bacteria, U.S. Food & Drug Administration (FDA)
• King & Prince Seafood Issues Voluntary Recall Notice On Breaded Calamari Products, U.S. Food & Drug Administration (FDA)
• Kanec USA, Inc. Issues a Voluntary Recall of Nite Rider Maximum Sexual Enhancer For Men and STUD Capsules for Men Male Enhancement Herbal Supplement Capsules Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• RECALL: Mama Rose's Con Queso, Hopi Corn Salsa -- Possible Botulism Risk, FoodSafety.gov
• Pretzels. Inc. Issues Allergy Alert On Undeclared Milk In Better Made Brand Corn Pops, U.S. Food & Drug Administration (FDA)
• FDA approves Viibryd to treat major depressive disorder, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Availability of the NARMS Strategic Plan, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fresenius Medical Care CombiSet True Flow Series Hemodialysis Blood Tubing Set with Priming Set and Transducer Protectors: Class I Recall - Potential for Kinking of Arterial Line, FDA MedWatch
• Hawaii Business Group Incorporated, Barb's Favorite Recipes, and Ohana Seafoods Recall Barb's Local Style Black Bean Sauce and Ohana Flavors Black Bean Sauce Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Mama Rose's Gourmet Foods Recalls Cilantro Con Queso, Garlic Con Queso, Viper Venom Con Queso and Hopi Corn Salsa Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Important Information for Betaseron® (interferon beta 1-b) Consumers Regarding Triad Group's Alcohol Prep Products, U.S. Food & Drug Administration (FDA)
• Maine seafood processor enters into consent decree with FDA, U.S. Food & Drug Administration (FDA)
• Rich Products Corporation announces nationwide voluntary recall of Sonny's Barbecue Deep Deveined Shrimp, U.S. Food & Drug Administration (FDA)
• Barrel O' Fun Snack Foods Co. Issues Allergen Alert on Undeclared Milk Protein in, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 19, 2011, U.S. Food & Drug Administration (FDA)
• FDA to improve most common review path for medical devices, U.S. Food & Drug Administration (FDA)
• RECALL: Toxic Waste® brand Nuclear Sludge® Chew Bars, FoodSafety.gov
• RECALL: Ossie's Schmaltz Herring, FoodSafety.gov
• RECALL: Winn-Dixie Beef Patties, OneGreat Hamburgers, FoodSafety.gov
• ALLERGY ALERT: Kroger Chocolate Chips Contain Milk, FoodSafety.gov
• FDA Approves Head Lice Treatment for Children and Adults, U.S. Food & Drug Administration (FDA)
• Commissioner's Fellowship Program, U.S. Food & Drug Administration (FDA)
• Federal government obtains permanent injunction against Deltex Pharmaceuticals Inc., U.S. Food & Drug Administration (FDA)
• Barry Callebaut USA LLC Issues Allergen Alert on Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips, U.S. Food & Drug Administration (FDA)
• Genentech Informs Customers Of Important Information About Triad Groups, U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products, U.S. Food & Drug Administration (FDA)
• MS Fish Corp Issues Alert On Listeria In, U.S. Food & Drug Administration (FDA)
• Multaq (dronedarone)- Risk of Severe Liver Injury:Reports include two cases of liver failure leading to liver transplant, FDA MedWatch
• December 2010 Safety Labeling Changes: 58 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Enforcement Report for January 12, 2011, U.S. Food & Drug Administration (FDA)
• Candy Dynamics Recalls Toxic Waste® brand Nuclear Sludge® Chew Bars, U.S. Food & Drug Administration (FDA)
• FDA seeks to halt processing, distribution at New York juice company, U.S. Food & Drug Administration (FDA)
• CVM Updates - January 2011 Update on Feed Enforcement Activities to Limit the Spread of BSE, U.S. Food & Drug Administration (FDA)
• Barry Callebaut USA LLC Issues Allergen Alert on Potential Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize dental devices from Florida manufacturer, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetaminophen Prescription Products Limited to 325 mg Per Dosage Unit: Drug Safety Communication, FDA MedWatch
• FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Webinar Announcement - Question-Based Review - Part III: Sterile Process Validation, U.S. Food & Drug Administration (FDA)
• The January 2011 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• Surtex Foods Recalls "Oaxaca String Cheese La Original" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Ground Beef Distributed to Institutions in CA and OR, FoodSafety.gov
• FDA MedWatch - Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL): Medication Use Error - Reports of Accidental Overdose, FDA MedWatch
• HIV/AIDS Update - Revised Adult HIV Treatment Guidelines available, U.S. Food & Drug Administration (FDA)
• AngioScore Incorporated Announces Worldwide Voluntary Field Removal of the AngioSculpt® PTA Scoring Balloon Catheter, 0.018" OTW, balloon sizes: 4.0x20mm, 5.0x20mm, and 6.0x20mm, U.S. Food & Drug Administration (FDA)
• La Placita Botanas Mexicanas, Inc. Recalls Wheat Snacks with Chile, Potato Chips with Chile, and Corn Churritos with Chile Because of Possible Contamination with Salmonella, U.S. Food & Drug Administration (FDA)
• FDA approves opioid analgesic to help cancer patients manage pain, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of lamivudine and tenofovir DF 300 mg/300 mg fixed-dose combination, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Working to Address Shortage of Injectable Iron Dextran - Status Update, U.S. Food & Drug Administration (FDA)