FDAFDA · Food and drugs·Recall number D-201-2013
Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724, NDC 0143-1176-01.
Published March 27, 2013 · Recall initiated: November 30, 2012
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: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV (C-IV)controlled substance. This product is being recalled because this controlled product was not relabeled with the required "C-IV" imprint on the label for products distributed after the 06/11/12 deadline.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- West-ward Pharmaceutical Corp.
- Distributor
- Nationwide
- Lot
- Lot #: 69160A
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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