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

XZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.

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

XZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.

Recalling firm
Schindele Enterprises dba Midwest Wholesale
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1340-2014

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.

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