FDAFDA · Food and drugs·Recall number D-299-2013
Pentrexcilina (acetaminophen, chlorpheniramine maleate, and phenylephrine HCl) tablets, 20-count tablets per carton, Distributed by: Laboratorios Norimex Co., San Diego, CA 92154, UPC 0 91965 02002 8.
Published May 1, 2013 · Recall initiated: April 12, 2013
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
Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading because they may be confused with Pentrexyl, a prescription antibiotic used to treat respiratory illnesses in Mexico.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- OPMX, LLC
- Distributor
- Nationwide
- Lot
- Lot #: 11611B0, Batch # 114039, Exp 10/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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