Watson Laboratories Inc recalls Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by
Recalled February 5, 2014 · FDA recall D-1053-2014 · Watson Laboratories
Hazard
Failed Tablet/Capsule Specifications; Product contains broken tablets. · FDA Class II
Units
717 bottles
Sold at
Nationally in: AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI.
Description
Failed Tablet/Capsule Specifications; Product contains broken tablets.
Product
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.
Manufacturer(s)
Watson Laboratories Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →