September 1, 2024

Night Bullet Dietary Supplement Recalled for Hazardous Ingredient

Green Plant, Inc. is recalling a product sold over the counter as a dietary supplement under the brand name "Night Bullet" because it contains trace amounts of an FDA-approved drug. The finished product contained trace amounts of Sulfohydroxyhomosildenafil and Aminotadalafil, which are analogues of sildenafil. Sildenafil is an FDA-approved active pharmaceutical ingredient used to treat erectile dysfunction (ED), which makes this product an unapproved drug. The batch lot number of the recalled product is B43N032, the UPC number is 018505122233, and expiration date is 10/2015. It was sold nationwide between October 2012 and March 2013 to wholesalers and samples provided at trade shows. If you purchased this product, immediately discontinue use. Contact your doctor if you experience any … [Read more...]

Maxiloss Weight Advanced Softgels Recalled for Sibutramine

Olaax Corp. is recalling the company's dietary supplement sold under the brand name Maxiloss Weight Advanced Softgels because they contain undeclared Sibutramine. FDA testing found the drug in the supplement. Sibutramine was a previously approved controlled substance that was removed from the market in October 2010 because it can substantially increase blood pressure and/or pulse rate in some patients. This may be a significant health risk to anyone with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. No illnesses or injuries have been reported to date. The recall includes all lot numbers and known to be counterfeit lot numbers of authentic lots. Any packaging types different from those listed are counterfeit. Any lot numbers not listed are … [Read more...]

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