Status
Terminated
Drug Enforcement D-1061-2013
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.
Classification
Class III
Report Date
September 25, 2013
Termination Date
July 25, 2014
Product Information
- 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.
- Product quantity
- 875 bottles
- 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.
- Recall initiation reason
- —
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Distribution pattern
- Nationwide
Location & Firm
- Recalling firm
- Watson Laboratories Inc
- Address
-
132 Business Center Dr, N/A
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-1061-2013
- Event ID
- 66169
- Recall initiation date
- August 30, 2013
- Center classification date
- September 17, 2013
- Code info
- Lot 706224A and 706225A, Exp. 04/15.
- More code info
- —