March 10, 2015, 2015 – Product Recall – Ultra ZX LABS, L.L.C. Issues Voluntary Nationwide Recall of Ultra ZX Since It Contains Undeclared Sibutramine and Phenolphthalein. For additional information, please refer to the company issued press release available on FDA’s web site at www.fda.gov/Safety/Recalls/UCM437517.
Posted by The U.S. Food and Drug Administration on 2015-03-10 16:55:47
Tagged: , UltraZx , Ultra ZX Labs , LLC , Drugs