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Eugene Oregon, Inc.

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20143
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FDA Recall Terminated Historical recordClass I

MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663

by Eugene Oregon, Inc.

Reason
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Published
October 8, 2014
Distribution
To retailers in MD, TX, FL, PA, IL, NJ,…

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FDA Recall Terminated Historical recordClass I

Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.

by Eugene Oregon, Inc.

Reason
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Published
October 8, 2014
Distribution
To retailers in MD, TX, FL, PA, IL, NJ,…

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FDA Recall Terminated Historical recordClass I

AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Road, Xining City.

by Eugene Oregon, Inc.

Reason
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Published
October 8, 2014
Distribution
To retailers in MD, TX, FL, PA, IL, NJ,…

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Showing 1–3 of 3 results

This page lists recalls that name Eugene Oregon, Inc. as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.