Eugene Oregon recalls
FDA enforcement reports naming Eugene Oregon, Inc. as the recalling firm.
- Recall reports
- 3
- Class I (serious)
- 3
- Most recent report
- Oct 8, 2014
- Oct 8, 2014AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioenginee…Drug · Eugene Oregon, Inc.Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.Class I
- Oct 8, 2014Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceuti…Drug · Eugene Oregon, Inc.Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.Class I
- Oct 8, 2014MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville,…Drug · Eugene Oregon, Inc.Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.Class I