Mojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed ...

FDA Recall #D-336-2013 — Class I — December 17, 2012

Recall #D-336-2013 Date: December 17, 2012 Classification: Class I Status: Terminated

Product Description

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;

Reason for Recall

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

Recalling Firm

Performance Plus Marketing, Inc. — Commerce, CA

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

219,000 capsules.

Distribution

Nationwide

Code Information

(1 count) Lot# 01MJ0712, (1 count) 01MM0211 Exp: 07/15; (5 count) Lot# 05M0912, Exp: 10/15;

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated