Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured By: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 00591-0540-05.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot #: 519406A, 521759A, Exp 04/14
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Watson Laboratories Inc
- Reason for Recall:
- Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured By: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 00591-0540-05.
Product Codes/Lot Numbers:
Lot #: 519406A, 521759A, Exp 04/14
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-058-2013
Related Recalls
Failed Tablet/Capsule Specifications; Product contains broken tablets.
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
Failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.