FDAFDA · Food and drugs·Recall number D-300-2013
Pentrexcilina Jarabe NF (dextromethorphan HBr and guaifenesin) liquid, 118 mL/ 4 fl oz bottle, Distributed by Laboratorios Nordimex Co., San Diego, CA 92154, UPC 0 91965 02001 1.
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 #: 11649A0, Exp 12/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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