D-1061-2013 Class III Terminated
FDA drug recall D-1061-2013 was initiated by Watson Laboratories Inc on August 30, 2013 and is designated Class III. Reason for recall: Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with. The recall status is terminated (terminated July 25, 2014). Affected quantity: 875 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- September 25, 2013
- Initiation Date
- August 30, 2013
- Termination Date
- July 25, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 875 bottles
Product Description
Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.
Reason for Recall
Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.
Distribution Pattern
Nationwide
Code Information
Lot 706224A and 706225A, Exp. 04/15.