FDAFDA · Food and drugs·Recall number D-0085-2025
ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com
Published December 11, 2024 · Recall initiated: November 4, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Boulla LLC
- Distributor
- Nationwide within the United States
- Lot
- Lot #: YZM240406, Exp: 04/05/2027
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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