FDAFDA · Food and drugs·Recall number D-1053-2014
Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by Watson Laboratories, Inc., Corona, CA 92880. Distributed by: Watson Pharma, Inc. NDC: 00591-0517-01.
Published February 5, 2014 · Recall initiated: January 15, 2014
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
Failed Tablet/Capsule Specifications; Product contains broken tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Watson Laboratories Inc
- Distributor
- Nationally in: AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI.
- Lot
- Lot #: 697316A, Expiry: Mar 2015.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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