Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

AFRICAN BLACK ANT Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil

Date: May 5, 2014
Company: Eugene Oregon, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Eugene Oregon, Inc. directly.

Affected Products

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

Quantity: 460 boxes

Why Was This Recalled?

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Where Was This Sold?

This product was distributed to 11 states: FL, IL, IN, LA, ME, MD, NJ, PA, SC, TX, WA

Affected (11 states)Not affected

About Eugene Oregon, Inc.

Eugene Oregon, Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report