Hydrocodone Bitartrate and Acetaminophen Tablets recall
Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA…
Why was Hydrocodone Bitartrate and Acetaminophen Tablets recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 706224A and 706225A, Exp. 04/15.
- Product
- Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA…
- Recalling firm
- Watson Laboratories Inc
- Quantity
- 875 bottles
- Distribution
- Nationwide
- Recall date
- September 25, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)