RecallWatchUSA

Home / Recalls / Drugs

Eugene Oregon, Inc. recalls AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Roa

Recalled October 8, 2014 · FDA recall D1612-2014 · Eugene Oregon

Hazard
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil. · FDA Class I
Units
460 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
AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Road, Xining City.
Manufacturer(s)
Eugene Oregon, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Eugene Oregon, Inc. recalls AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Roa | RecallWatchUSA