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Update to Voluntary Recall of Eliquis® (apixaban) 5 mg Tablets (#HN0063) - Recall to retail/dispensing level only

June 17, 2017, 3:35 am by FDA Recalls

On June 10, Bristol-Myers Squibb announced a voluntary recall of one lot (#HN0063) of Eliquis 5 mg tablets. This lot was distributed nationwide in the U.S. to wholesalers and retail pharmacies in February 2017. Bristol-Myers Squibb is taking this precautionary measure based on a single customer complaint that a bottle labeled as Eliquis5 mg was found to contain Eliquis 2.5 mg tablets. No other lots are impacted by this recall.


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Magno-Humphries Laboratories, Inc., Issues Voluntary Nationwide Recall of Basic Drugs Brand of Senna Laxative Due to Mislabeling
FDA Recalls : January 22, 2018, 7:38 am
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
FDA Recalls : January 22, 2018, 7:37 am
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.

Sun Noodle - New Jersey - Issues Allergy Alert on Undeclared Fish in Tonkotsu Ramen
FDA Recalls : January 22, 2018, 7:09 am
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
FDA Recalls : January 22, 2018, 1:47 am
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.

Break Ventures/California Basics Recalls "Zero For Him" 150ct Lot#1710-638 Because of Possible Health Risk
FDA Recalls : January 21, 2018, 1:49 am
Break Ventures/California Basics is recalling its Dietary Supplement "Zero for Him 150ct" Lot#1710-638(the "Product") because it may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.