Performance Plus Marketing, Inc. recalls BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution

Recalled May 22, 2013 · FDA recall D-334-2013 · Performance Plus Marketing

Hazard

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

Units

213,000 capsules

Sold at

Nationwide

Description

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

Product

BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution Los Angeles, CA 90026. 1 count blister: UPC 705105524764, 5 count blister: UPC 736211124012, 10 count blister: UPC 736211123916.

Manufacturer(s)

Performance Plus Marketing, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →