- Regulatory Science Update: FDA and International Serious Adverse Events Consortium Complete Third Data Release
- Queseria Bendita Recalls Queso Fresco, Panela, and Requeson Because of Possible Health Risk
- Lovin Oven LLC Voluntarily Recalls Certain Health Valley® Organic Peanut Crunch, Dutch Apple And Wildberry Chewy Granola Bars
- FDA Announces Possible Safety Concern for HIV Drug Combination
- U.S. Attorney News Release: Woman pleads guilty to poisoning salsa at Lenexa restaurant
- NIH and FDA Announce Collaborative Initiative to Fast-track Innovations to the Public
- FDA Approves Pneumococcal Disease Vaccine with Broader Protection
- Maryland Veal Calf Dealer Agrees to Close in Response to FDA-Initiated Action
- U.S. Attorney News Release: Medical Technician Sentenced to 30 Years
- Wholesome Spice Recalls 25 Lb. Boxes Of Crushed Red Pepper Because Of Possible Health Risk
- Trader Joe's Company Voluntarily Recalls Chocolate Chip Chewy Coated Granola Bars
- FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 25, 2010
- LifeScan Recalls Specific Lots of Consumer and Professional OneTouch® SureStep® Test Strips Due To Inaccurate
- Thumb Oilseed Recalls Soy Grits and Flour Because of Possible Health Risk
- U.S. Attorney News Release: Medical Device Manufacturer Guidant Charged in Failure to Report Defibrillator Safety
- FDA Approves Therapy to Treat Gaucher Disease
- American Pecan Co. Recalls Pecans Because of Possible Health Risk
- International Collaboration: FDA and European Medicines Agency Agree to Accept a Single Orphan Drug Designation Annual Report
- FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 26, 2010
- Johnny's Fine Foods Recalls Johnny's French Dip Powdered Au Jus Because of Possible Health Risk
- FDA Announces Meeting Information and Voting Membership of the Tobacco Products Scientific Advisory Committee
- Heartland Foods, Inc. voluntarily recalls Coarse Ground Black Pepper because of possible Salmonella Contamination
- T. Marzetti Company Announces a Voluntary Recall of Dips Due to Possible Health Risk
- U.S. Attorney News Release: Boca Raton Man Sentenced for Nutritional Supplement Scam
- FDA Approves First Generic Tamsulosin to Treat Enlarged Prostate Gland
- FDA Survey Finds More Americans Read Information on Food Labels
- Castella Imports, Inc. Conducts Nationwide Recall of Castella Chicken Soup Base Because of Possible Health Risk
- Tim's Cascade Snacks Recalls 'Hawaiian® Kettle Style Potato Chips - Sweet Maui Onion' and 'Hawaiian- Sweet Maui Onion Rings' Because of Possible Health Risk
- FDA Calls on Food Companies to Correct Labeling Violations; FDA Commissioner Issues an Open Letter to the Industry
- FDA, FSIS, CDC Collaborate on Methods to Measure Success of Food Safety Programs
- FDA Warns Consumers in Puerto Rico of Harmful Bacteria in Hand Sanitizers
- La FDA advierte a los consumidores en Puerto Rico acerca de la presencia de una bacteria dañina en desinfectantes para manos
- Homemade Gourmet Voluntarily Recalls Tortilla Soup Mix Because of Possible Health Risk
- Earth Island Announces Voluntary Recall On Select Follow Your Heart Products That Contain Natural Flavor Because Of Possible Health Risk
- Reser's Fine Foods Inc Press Release
- FDA Approves Name Change for Heartburn Drug Kapidex
- FDA Investigation Reveals Salmonella Tennessee at Plant that Makes Flavor Enhancers for Food Processors and Other Distributors
- Concord Foods Recalls Concord Foods Seasonings Mixes because of Possible Health Risk
- Creative Contract Packaging Corporation Recalls HERB-OX® Bouillon Products Because of Possible Health Risk
- FDA Update on the Investigation into the Salmonella Montevideo Outbreak - March 5, 2010
- Fresh Food Concepts Announces a Voluntary Recall of Spinach Dips Due to Possible Health Risk
- McCormick Company Initiates Recall Due to Possible Health Risk from HVP Ingredient
- Ed Roller, Inc. Announces Voluntary Recall of Wegmans 9 oz. Food You Feel Good About® Medium Seafood Sauce Due to Undeclared Ingredients on Label
- Mincing Overseas Spice Company Voluntarily Recalls Two Lots of Black Pepper
- National Pretzel Co. Annouces Precautionary Recall of Honey Mustard Onion Seasoned Pretzels Because of Possible Health Risk
- Estrella Family Creamery Recalls Old Apple Tree Tomme Cheese Due to Possible Health Risks
- GNS Foods Voluntarily Recalls Snack Mixes Containing Honey Mustard/Onion Pretzels from National Pretzel Co. associated with Hydrolyzed Vegetable Protein (HVP) recalled by Basic Food Flavors, Inc. because of the potential Salmonella contamination.
- Nature's Variety Expands Nationwide Voluntary Recall to Include All Raw Frozen Chicken Diets with Any Best If Used By Date On or Before 2/5/11
- Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Black Pepper and Products made with Black Pepper
- FDA Approves Botox to Treat Spasticity in Flexor Muscles of the Elbow, Wrist and Fingers
- Herr Foods Inc. Recalls 'Herr's Cracked Pepper and Sea Salt Flavored' Kettle Style Potato Chips Because of Possible Health Risk
- Nutritional Resources Announces a Nationwide Voluntary Recall of Healthwise Cream of Mushroom Soup Due to Possible Health Risk
- PG Joins Industry Ingrent Recall by Voluntarily Recalling Two Flavors of Pringles® in the United States in Response to FDA Industry Guidance
- Kroger Recalls Two Onion Soup Dip Mixes Due to Possible Health Risk
- Publix Issues Voluntary Recall on Four Seasoning Mixes
- Ventura Foods, LLC Voluntarily Recalls Seven Varieties of Its Dean’s® Dip Products As A Precautionary Measure
- Olde Westport Spice Announces a Voluntary Recall of Garden Harvest Special Blend Seasoning
- Quaker Snack Mix Baked Cheddar Voluntarily Recalled Due to Possible Health Risk
- Mrs. Gerry’s Kitchen Press Release.
- Mrs. Gerry’s Kitchen Press Release
- Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Black Pepper
- Orval Kent Food Company, Inc. Voluntarily Recalls Culinary Circle Dips Due to Possible Health Risk
- FDA March 11 Update on the Investigation into the Salmonella Montevideo Outbreak
- Austinuts Of Dallas, Inc. Announces Voluntary Recall of Honey Mustard Pretzels
- McCormick Recall Due to Possible Health Risk from HVP Ingredient Expands to Include Additional Best By Dates
- FDA Issues Warning on Counterfeit Surgical Mesh
- FDA Task Force Seeks Public Comments on Increasing Transparency with Regulated Industry
- FDA Announces New Boxed Warning on Plavix
- Julia's Spices Inc Recalls Hulled Sesame Seeds Because of Possible Health Risk
- Spice Industrial Inc. Recalls Lian How White Sesame Seeds Because of Possible Health Risk
- Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters
- Tastefully Simple Issues Voluntary Recall for Toasted Garlic Parmesan Cheese Ball Mix
- Emmi - Roth Käse USA Announces Recall of Spreadables brand Crab Creole and Shrimp Scampi Cheese Spreads
- GFN Foods, LLC Voluntarily Recalls Gluten-Free Naturals Pancake Mix, Gluten-Free Naturals Light Moist Yellow Cake Mix and Gluten-Free Naturals Cookie Blend Flour
- FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets
- Barcel Announces Voluntary Recall
- Produce Valley, Inc. Initiates Voluntary Recall Due to Possible Health Risk Associated with Recalled Hydrolyzed Vegetable Protein (HVP) by Basic Food Flavors, Inc.
- FDA Seeks Permanent Injunction Against Louisiana Sprout Grower
- FDA March 17 Update on the Investigation into the Salmonella Montevideo Outbreak
- FDA Approves First Totally Implanted Hearing System
- Statement for National Poison Prevention Week
- C. H. Guenther Son, Inc. Announces Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk
- The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter
- Spice Barn, Inc. Voluntarily Recalls Two Lots of Black Pepper
- FDA Approves Drug to Treat Condition That Causes Elevated Ammonia Levels
- FDA Warns about Increased Risk of Muscle Injury with Zocor
- Kroger Amends Code Date on Recalled Seasoning Blend Garlic Powder
- John B. Sanfilippo Son, Inc. Voluntarily Recalls Snack Mix and Cashew Products Due to Possible Health Risk
- U.S. Attorney News Release: Springfield (Missouri) Business Owner Pleads Guilty to $17 Million Fraud Scheme
- Components of Extraneous Virus Detected in Rotarix Vaccine; No Known Safety Risk
- U.S. Attorney News Release: Three Indicted for Diversion of Prescription Drugs
- C. H. Guenther Son, Inc. Announces Amended Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk
- McCain Foods USA Announces Voluntary Recall of Frozen Potato Product Containing Black Pepper That May Pose Health Risk
- U.S. Attorney News Release: Nurse Sentenced to 30 Months in Prison for Tampering with a Consumer Product
- Walong Marketing, Inc. Expands Nationwide Voluntary Recall Flying Horse Sesame Chewy Candy Due to Undeclared Peanuts
- Blue Line Foodservice Distribution voluntarily recalls “Spice Paks”
- FDA Approves New Use of Xifaxan for Patients with Liver Disease
- C. H. Guenther Son, Inc. Announces Amended Voluntary Nationwide Recall of several additional products that contain pepper due to Possible Health Risk
- C. H. Guenther Son, Inc. Announces Voluntary Nationwide Recall of Chilli Man Seasoning Mix due to Possible Health Risk
- Obstetrics Manager Convicted of Tampering with Patient's Narcotics Medicines at White Salmon Hospital
- FDA Takes Action Against New York Dairy Farmer
- Public Health Agencies Warn of Outbreaks Related to Drinking Raw Milk
- Two Arrested for Illegally Trafficking Counterfeit Weight Loss Medication
- Public Health Agencies Collaborate to Prevent Further Illnesses from Norovirus Outbreak Associated with Oysters Recently Harvested from Area Near Port Sulphur, La.
- Perfect Candy Packaging Co. Announces a Voluntary Nationwide Recall of Whole Black Pepper in H.D.W. FOODS Labeled Bags
- Modern Products recalls Seasonings due to possible health risk
- Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed As a Dietary Supplement
- FDA Approves Asclera to Treat Small Varicose Veins
- Bass Pro Shops® Announces Voluntary Nationwide Recall of Uncle Bucks® Beer Batter Mix Lightly-Seasoned 20 oz. Canisters containing potentially contaminated pepper due to possible health risk.
- Binell Bros. Cutlery Voluntarily Recalls Black Pepper
- Bass Pro Shops® Announces Voluntary Nationwide Recall of Uncle Bucks® Beer Batter Mix Lightly-Seasoned 20 oz. Canisters containing potentially contaminated pepper due to possible health risk
- FDA Requires Device Manufacturers to Include Information on Pediatric Populations
- Lance, Inc. Has Issued a Voluntary Recall of All Tom's Barbecue Potato Chips Because Of A Possible Health Risk
- Federal Government Seeks Permanent Injunction Against Texas Egg Roll Manufacturer
- Watkins Incorporated Recalls Crab Snack Dip Seasoning Because of Possible Health Risk from Ingredient Supplied by Kerry Ingredients
- Zatarain's Recalls Original Dirty Rice Mix Package Due to Unlabeled Wheat and Barley Ingredients
- Glutino Food Group Issues Allergy Alert on Undeclared Egg Product in Raisin Bread
- NY Gourmet Salads Inc. Recalls Chick Pea Salad Because of Possible Health Risk
- Golden Pacific Foods, Inc. Issues Allergy Alert for Undeclared Milk and Soy in Marco Polo Brand Shrimp Snacks
- FDA Approves First Biodegradable Sealant Patch for Cardiovascular Surgery
- Federal Government Seizes Dozens of Misbranded Drug Products
- FDA Approves New Formulation for OxyContin
- Kanec USA Inc., Issues a Voluntary Nationwide Recall of Stud Capsule For Men Marketed as Dietary Supplements
- Whole Foods Market Voluntarily Recalls Frozen Whole Catch Yellow Fin Tuna Steaks Due to Possible Health Risks
- Del Bueno Recalls Queso Fresco Because of Possible Health Risk
- Kroger Recalls Two Seasonings Due to Possible Health Risk
- Del Bueno Amends Recall of Queso Fresco Cheese Because of Possible Health Risk
- FDA Issues Warning Letters for Drugs Promoted in Fat Elimination Procedure
- Medical Device Manufacturer Guidant Pleads Guilty for not Reporting Defibrillator Safety Problems to FDA
- US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles.
- FDA Approves First Generic Versions of Two Drugs for the Treatment of Hypertension
- Mccormick Company Recalls Mccormick Fajitas Seasoning Mix Due To Unlabeled Wheat And Milk Ingredients
- FDA Provides Information to Consumers about Triclosan
- FDA Holds Public Meeting on Prescription Drug User Fee Act
- Consumer Alert Precautionary Recall issued for H-E-B French Onion Dip
- FDA Approves Pancreatic Enzyme Product, Pancreaze
- Response Products Voluntarily Recalls Advanced Cetyl M Joint Action Formula for Dogs Because of Possible Salmonella Health Risk
- Asthma and COPD Inhalers That Contain Ozone-depleting CFCs to be Phased Out; Alternative Treatments Available
- Atlas Operations, Inc. Announces Expansion of its Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements
- My-A Co, Recalls Ground Black Pepper Double Golden Fish 3.5oz Jars Due to Salmonella Contamination
- FDA Issues Guidance on New Safety Rules for Shell Eggs
- StarKist Co. Initiates Limited Regional Voluntary Recall of Two SeaSations® Products Due to Undeclared Allergen
- ***CONSUMER ALERT*** Undeclared Sulfites in Nut Tree Health Mix
- FDA Seeks Injunction Against Florida Animal Drug Compounder
- FDA Launches Medical Device and Radiation-Emitting Product Transparency Web site
- Purina Mills Undertakes Limited Recall of Strategy® Horse Feed and Layena® Poultry Feed
- FDA to Address Challenges of Using Complex Medical Devices in the Home
- FDA Statement on IOM Sodium Report
- FDA Obtains Consent Decree to Stop Marketing of Unapproved Sterilization System
- FDA Announces Draft Revised Guidance on Transparency and Advisory Committees
- Buckley Woman Sentenced to Jail Time, Home Detention for False Claim of Glass in Bottled Water
- Federal Prisoner Serving Time for Health Care Fraud Charged with Distributing Misbranded Drugs that were Labeled as All Natural Sexual Enhancement
- FDA Launches Initiative to Reduce Infusion Pump Risks
- Covidien Initiates Voluntary Recall of Certain Shiley? Tracheostomy Tubes
- Two Arrests Made in Contaminated Food Case
- FDA Changes Process for Medical Device Advisory Committees
- FDA Warns Users about Faulty Components in 14 External Defibrillator Models
- FDA Approves New Device for Adults with Severe and Persistent Asthma
- MiDAS Foods International Recalls Instant Beef Soup Mix and Instant Beef Stroganoff Sauce Mix Because Of Possible Health Risk
- FDA Seeks Comment, Information, Data on Front-of-Package Labeling and Shelf-Tag Symbols
- FDA Urges Industry to Take Additional Steps to Prevent Cargo Theft
- FDA Approves a Cellular Immunotherapy for Men with Advanced Prostate Cancer
- FDA Offers Consumer Tips about Shopping at the Store on FoodSafety.gov
- FDA Takes Steps to Increase Safety of Foods During Transport
- Humei Trading Inc. Issues Alert on Undeclared Sulfites in Dried Pachyrhizus, Product of China
- Northern Food I/E Issues Alert on Undeclared Sulfites in Havista White Fungus
- FDA Approves Chagas Disease Screening Test for Blood, Tissue and Organ Donors
- McNeil Consumer Healthcare Announces Voluntary Recall of Certain OTC Infants’ and Children’s Products
- McNeil Recalls Infant and Children’s Liquid Products Including Tylenol and Motrin
- FDA Warns Consumers to Avoid Vita Breath Dietary Supplement
- FDA Conducting Safety Review of Commonly Used Prostate Cancer Drugs
- FDA Issues Statement on Baxter’s Recall of Colleague Infusion Pumps
- Longmont Man Sentenced for Removing and Replacing Labels on Gatorade Bottles
- Nestlé USA Announces Voluntary Recall on Nestlé Carnation Famous Fudge Kits due to Incomplete Allergen Labeling
- Freshway Foods Voluntarily Recalls Products Containing Romaine Lettuce Because of Possible Health Risk
- Teleflex Medical Announces Worldwide Voluntary Recall of Teleflex Medical AQUA+FLEX Hygroscopic Condenser Humidifier (Catalog Number 1570)
- FDA Supports Freshway Foods Voluntary Recall
- FDA Approves New Combination Product Oral Contraceptive
- Imported Manouri Cheese Voluntarily Recalled due to Potential Listeria Contamination
- Federal and State Officials Confirm Link Between Bagged Romaine Lettuce and E. coli O145 Illness Outbreak
- FDA: ?Bad Ad Program? to Help Health Care Providers Detect, Report Misleading Drug Ads
- FDA: Serious Side Effects from Swallowing Topical Benadryl Product
- Minnesota Firm Issues Recall Due to Undeclared Dairy Allergen in Certain Sunflower Seeds
- Baroody Imports, Inc. Issues Allergy Alert on Undeclared Sulfites in Baroody Dried Apricots
- FDA Revises Recommendations for Rotavirus Vaccines
- York Man Federally Sentenced for Prescription Drug Fraud Conspiracy
- Amish Wedding Recall Press Release
- Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, USP 500 mg/100 mL
- Dominguez Family Enterprises Issues Allergy Alert on Mexican Bread Product
- FDA Transparency Task Force Unveils Draft Proposals on Agency Disclosure Policies
- Louisville Man Pleads Guilty to Distributing 2CE
- Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in Gourmet Cookie Mixes
- Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Egg in Peanut Butter Spread
- Vanlaw Food Products, Inc. Announces Voluntary Recall of Valu Time Brand Ranch Dressing
- Voluntary Recall of HYLENEX Initiated
- Caldwell Fresh Foods Recalls Alfalfa Sprouts Because of Possible Health Risks
- Urgent Nationwide Alfalfa Sprout Recall
- FDA Clears First 2009 H1N1 Influenza Virus Test Previously Approved for Emergency-Use Only
- Ortho-McNeil Pharmaceutical, LLC Pleads Guilty to Illegal Promotion of Topamax and is Sentenced to Criminal Fine of $6.14 Million
- Genzyme Corp. Signs Consent Decree to Correct Violations at Allston, Mass., Manufacturing Plant and Give up $175 Million in Profits
- FDA and NIH Launch Electronic Safety Reporting Portal
- Fresh Express Recalls Romaine-based Salads with Use-by Dates of May 13-16th Due to Possible Health Risk
- FDA Approves New Treatment for Late-Onset Pompe Disease
- FDA: Possible Fracture Risk with High Dose, Long-term Use of Proton Pump Inhibitors
- Western District of Wisconsin Announces Consent Decree Between Beehive Botanicals and the United States
- FDA Announces Collaboration with Drugs.com
- FDA: Rare Cases of Liver Injury Reported with Use of Xenical, Alli
- So Shing Hing (USA) Trading Co Ltd Issues an Alert on Undeclared Sulfites in Dried Melon
- Herb And Honey Issues Alert On Undeclared Sulfites In Dried Apricots
- FDA Warning: Consumers Advised Not to Use Arrow Brand Medicated Oil -Embrocation, Aceite Medicinal La Flecha, or ??????
- Wally's Nut House, LLC ISSUES ALLERGY ALERT ON UNDECLARED MILK, SOY, AND WHEAT IN THE FOLLOWING PRODUCTS: Tailgate Crunch Mix, Sweet Cajun Heat Mix, Country Western Mix, Cranberry Raisin Mix, Party Mix, Hot 'n Spicy Mix, and Louisiana Cajun Mix
- Wally's Nut House, LLC Issues Allergy Alert on Undeclared Milk, Soy, and Wheat
- organicgirl Produce Announces Limited Precautionary Recall of 10 oz organicgirl Baby Spinach with Use-by Date of May 22 Due to Possible Health Concern
- Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn? and Propofol That May Contain Particulate Matter
- Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children's Products
- Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks
- FDA Approves New Injectable Osteoporosis Treatment for Postmenopausal Women
- Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.
- Kent Nutrition Group, Inc. Undertakes Limited Recall of Kent Feeds 20 Lamb DQ45 Medicated
- FDA Takes Action Against California Soy-Product Manufacturer Lifesoy
- Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico
- Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
- West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk
- Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
- Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED® and ReviveR AEDTM
- PG Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1)
- FDA Advisory Panel to Review Dental Amalgam
- FDA Seizes More Than $32,000 Worth of Bulk Honey from Philadelphia Distribution Center
- Domega NY International Co., LTD Issues Allergy Alert on Undeclared Egg in Fuma Custard Pie
- Former Colorado Springs Pharmacist Sentenced for Importation and Distribution of Chinese-Made Human Growth Hormones and Conspiracy to Distribute Anabolic Steroids
- Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk
- Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen
- NOAA, FDA Continue Ramping Up Efforts to Ensure Safety of Gulf of Mexico Seafood
- Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes
- Portland Shellfish Company Recalls Cooked, Frozen Claw Island Brand, Craig’s All Natural Brand And Inland Ocean Brand Lobster Claw And Knuckle Meat Because Of Possible Health Risk
- FDA Cautions on Accurate Vitamin D Supplementation for Infants
- FDA to Communicate Safety Monitoring Activities to Consumers and Health Care Professionals
- FDA to Host Public Meeting on Oversight of Laboratory-Developed Tests
- Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab™ Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count
- FDA Approves New Treatment for Advanced Prostate Cancer
- FDA Warns About Fraudulent Tamiflu
- FDA Fines American Red Cross $16 Million for Prior Failures to Meet Blood Safety Laws
- FDA Approves New Indication for Tasigna
- Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products
- Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato Chicken Dry Dog Food Due to a Possible Health Risk
- Rich Products Corporation announces nationwide voluntary recall of Allen Bavarian Crème Filling due to undeclared allergens in product
- FDA Warns Consumers to Avoid Magic Power Coffee
- FDA Approves First Diagnostic Assay to detect both HIV Antigen and Antibodies
- Portland Shellfish Company Expands Recall to Include Meat Without Feet Label, Lobster Claw and Knuckle Meat, because of Possible Health Risk
- FDA Marks First Anniversary of Tobacco Control Act