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.

libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to Undeclared Sildenafil

Date: December 17, 2012
Company: Performance Plus Marketing, 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 Performance Plus Marketing, Inc. directly.

Affected Products

libigrow capsules, PERFORMANCE ENHANCER, supplied in 1, 5 and 10 count blister packs, Distributed By: H & K Nutraceuticals Los Angeles, CA 1 count blister: UPC 094922567611, 5 count blister: UPC 094922567628, 10 count blister: UPC 610585434253.

Quantity: 610,000 capsules

Why Was This Recalled?

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Performance Plus Marketing, Inc.

Performance Plus Marketing, Inc. has 7 total recalls tracked by RecallDetector.

Related Recalls

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