FDAFDA · Food and drugs·Recall number D-1042-2016
VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
Published June 29, 2016 · Recall initiated: May 11, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Profarma Distributors LLC
- Distributor
- Nationwide
- Lot
- Lot # UJE 040; Exp. 02/17
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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