US Drug Recall Register
Class I · High risk Terminated Initiated Jul 16, 2012 (14 years ago)

Z-ROCK All Natural Male Supplement. 1 capsule blister pack, UPC 0 00309 50792 7…

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

Why it was recalled

Marketed Without an Approved NDA/ANDA: Products tested positive for Sildenafil and analogs of Sildenafil.

What was recalled

Z-ROCK All Natural Male Supplement. 1 capsule blister pack, UPC 0 00309 50792 7, Distributed by Zrock USA PO Box 668297, Pompano Beach, FL 33066

Recalling firm
Coral Rock Man, Inc.
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-039-2013

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.