Performance Plus Marketing, Inc. recalls Mojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed By: Mojo Health, Pompan

Recalled May 22, 2013 · FDA recall D-336-2013 · 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

219,000 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

Mojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed By: Mojo Health, Pompano Beach, FL I count blister UPC - 718122119738; 5 count blister UPC - 705105836430;

Manufacturer(s)

Performance Plus Marketing, Inc.

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