RecallWatchUSA

Home / Recalls / Drugs

Performance Plus Marketing, Inc. recalls Mojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distri

Recalled May 22, 2013 · FDA recall D-337-2013 · 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
70,000 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 SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distributed By: Mojo Health, Pompano Beach, FL
Manufacturer(s)
Performance Plus Marketing, Inc.

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

Performance Plus Marketing, Inc. recalls Mojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distri | RecallWatchUSA