US Drug Recall Register
Class I · High risk Terminated Initiated Jan 9, 2014 (13 years ago)

XZONE GOLD, 1 capsule blister 750 mg, Distributed by: XZONE, Orlando, FL.

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

Why it was recalled

Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.

What was recalled

XZONE GOLD, 1 capsule blister 750 mg, Distributed by: XZONE, Orlando, FL.

Recalling firm
Schindele Enterprises dba Midwest Wholesale
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1334-2014

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.

Other Gold recalls

See all