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Recall Observatory FDA recall evidence

Drug product

Xzone 1200, 750 mg, one capsule per blister pack, Distributed by: Xzone, Orlando, FL 32789

D-1601-2014

March 28, 2014

Class I

Product summary

Firm
Nova Products, Inc.
Event
Event 67860
Status
Terminated
Classification
Class I
Quantity
Unknown
Official record key
drug-enforcement:D-1601-2014

Official wording

Reason: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylvania is voluntarily recalling XZone 1200because FDA laboratory analysis determined that they contain undeclared amounts of sildenafil and tadalafil, active ingredients of FDA-approved drugs used to treat erectile dysfunction.

Code information: Lot# 13071012

Distribution pattern: Nationwide to retailers and distributors

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylvania is voluntarily recalling XZone 1200because FDA laboratory analysis determined that they contain undeclared amounts of sildenafil and tadalafil, active ingredients of FDA-approved drugs used to treat erectile dysfunction.