FDA recall D-1334-2014

Schindele Enterprises dba Midwest Wholesale · Class I · drug

Product

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

Reason for recall

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

Distribution

Distributed to PA, IL, TX, IA, GA, CT, FL, CA, LA, NY, MD, NV, and WI

Key facts

Status
Terminated
Initiation date
2014-01-09
Report date
2014-05-28
Termination date
2015-02-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Nixa, MO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1334-2014