Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hydrocodone Bitartrate and Acetaminophen Tablets USP Recalled by Watson Laboratories Inc Due to Failed Tablet/Capsule Specifications; Product contains broken tablets.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Watson Laboratories Inc directly.
Affected Products
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.
Quantity: 717 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications; Product contains broken tablets.
Where Was This Sold?
This product was distributed to 10 states: AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI
About Watson Laboratories Inc
Watson Laboratories Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report