Eugene Oregon, Inc. recalls Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
Recalled October 8, 2014 · FDA recall D-1613-2014 · Eugene Oregon
Hazard
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil. · FDA Class I
Units
136 boxes
Sold at
To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
Description
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Product
Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
Manufacturer(s)
Eugene Oregon, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →