US Drug Recall Register
Class I · High risk Terminated Initiated Dec 17, 2012 (14 years ago)

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

Class I — High risk. Reasonable probability of serious harm or death.

Why it was 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

What was recalled

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;

Recalling firm
Performance Plus Marketing, Inc.
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-336-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.