Eugene Oregon Recalls
3 recalls on record · October 8, 2014 to October 8, 2014 · Drugs
October 8, 2014DrugsFDA
Eugene Oregon, Inc. recalls MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
Hazard: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
October 8, 2014DrugsFDA
Eugene Oregon, Inc. recalls Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
Hazard: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
October 8, 2014DrugsFDA
Eugene Oregon, Inc. recalls AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Roa
Hazard: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.