FDAFDA · Food and drugs·Recall number D-058-2013
Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured By: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 00591-0540-05.
Published November 28, 2012 · Recall initiated: September 21, 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
Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Watson Laboratories Inc
- Distributor
- Nationwide
- Lot
- Lot #: 519406A, 521759A, Exp 04/14
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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