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Hydroxycut is a brand of dietary supplements that is marketed as a weight loss aid. Hydroxycut was originally developed and manufactured by MuscleTech Research and Development; MuscleTech was sold to Iovate Health Sciences in 2003–2004 and declared bankruptcy in 2005; Iovate continues to use MuscleTech as a brand to market Hydroxycut.
MuscleTech is a brand of dietary supplements, marketed by Iovate Health Sciences Inc., which includes Hydroxycut. It was owned by Canadian company Kerr Holdings which was acquired by the Xiwang Foodstuffs Company, a Chinese company, for $584 million in 2016.
On May 1, 2009, the FDA issued a warning to consumers to stop using Hydroxycut products, due to 23 reports of serious health problems associated with the use of Hydroxycut, and at least one death. The FDA cited a total of 23 case reports of Hydroxycut-associated liver toxicity in their CAERS database over a seven year period from 2002 to the ...
A glitch in a version of Tandem Diabetes Care's Apple iOS app that is used with certain insulin pumps has led to over 200 injuries, prompting the FDA to issue a recall.
Viatris Inc's (NASDAQ: VTRS) Mylan will pull one batch of non-interchangeable Semglee, also known as insulin glargine injection. The Company cited the risk of the label is missing on some ...
2021 – Butterball recalled over 14,000 lbs of turkey meat due to suspected plastic contamination. [109] [110] 2022 – Abbott Nutrition recalled Similac baby formula after the death of an infant from Cronobacter sakazakii. [111] The recall caused significant shortages in baby formula across the United States. [112]
Consumers who purchased the recalled bars should return for a refund. Customers with questions can call Riverside at 855-215-5695 between 8 a.m. and 5 p.m. Eastern Time. Extended interview: Billie ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]