FDA approves first radioactive drug for a certain type of digestive tract cancer called GEP-NETs
Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA’s strengthened commitments to humane and judicious animal research and the termination of a nicotine study
FDA strengthens commitments to humane and judicious animal research and the termination of a nicotine study
Bulletproof 360, Inc. Issues Allergy Alert on Undeclared Milk in Collagen Protein Dietary Supplement
Out of an abundance of caution, Bulletproof 360, Inc. is voluntarily recalling one lot #1017088 of Bulletproof Collagen Protein dietary supplement due to undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.
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National Frozen Foods Corporation Recalls Frozen Green Beans and Frozen Mixed Vegetables Because of Possible Health Risk
National Frozen Foods Corporation (NFFC) is voluntarily recalling a limited quantity of Not-Ready-To Eat Individually Quick Frozen (IQF) green beans and IQF mixed vegetables because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
FDA, FTC warn companies for selling illegal, unapproved opioid cessation products using deceptive claims
FDA and FTC issued joint warning letters to the marketers and distributors of 12 opioid cessation products, for illegally marketing unapproved products with claims about their ability to help in the treatment of opioid addiction and withdrawal
Products Pacheco Inc Issues Allergy Alert For Undeclared Wheat, Soy, Egg, Milk and Undeclared Artificial Coloring in its Bakery Products
PRODUCTS PACHECO INC. in Bayamón, Puerto Rico, is recalling the following products of PACHECO brand because they may contain undeclared allergens: Wheat, Soy, Egg, Milk and artificial coloring not listed: Red#40, Yellow#5, Yellow#6. People who have allergies to these foods run the risk of serious or life-threatening allergic reaction if they consume these products
Sun Noodle – New Jersey – Issues Allergy Alert on Undeclared Fish in Tonkotsu Ramen
Sun Noodle of Carlstadt, NJ is voluntarily recalling one lot of their retail Tonkotsu Ramen because it is mis-labeled. While it is labeled Tonkotsu, the actual flavor packet inside is Assari Shoyu, which contains an additional undeclared allergen of fish (sardines).
Productos Pacheco Inc Emite La Alerta De Alergenos No Declarados: Trigo, Soya, Huevo, Leche Y Colorantes No Declarados En Sus Productos De Panaderia
PRODUCTOS PACHECO INC. en Bayamón, Puerto Rico, está recogiendo los siguientes productos marca PACHECO porque pueden contener alérgenos no declarados: Trigo, Soya, Huevo, Leche y colorantes artificiales no listados en ingredientes Rojo#40, Amarillo#5, Amarillo#6. Las personas que tienen alergias a estos alimentos y colores artificiales corren el riesgo de una reacción alérgica grave o que pone en peligro la vida si consumen estos productos.
Magno-Humphries Laboratories, Inc., Issues Voluntary Nationwide Recall of Basic Drugs Brand of Senna Laxative Due to Mislabeling
Tigard, OR, Magno-Humphries Laboratories, Inc., is voluntarily recalling one lot of Basic Drugs Brand of Senna Laxative tablets, 8.6mg Sennosides to the consumer level due to a customer complaint that their bottle labeled as Senna Laxative actually contained Basic Drugs Brand of Naproxen Sodium 220mg. Naproxen Sodium 220mg tablet is used as a pain reliever and is a nonsteroidal anti-inflammatory drug (NSAID).
Flawless Beauty, LLC Issues Voluntary Recall of Unapproved Drugs
Ocean Township, NJ. In accordance with a Consent Decree of Permanent Injunction ordered in the United States District Court for the District of New Jersey, Flawless Beauty, LLC is voluntarily recalling all lots of nineteen different products sold individually or as part of multi-unit kits alleged by the U.S. Food and Drug Administration (“FDA”) to be misbranded or unapproved new drugs pursuant to the Federal Food, Drug, and Cosmetic Act. The FDA believes that these drugs present serious public health risks.