Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Oxycodone and Acetaminophen Tablets Recalled by Watson Laboratories Inc Due to Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP...
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
Oxycodone and Acetaminophen Tablets, USP 10 mg/650 mg, CII, 100 Count Bottles, Rx Only, Manufactured by: Watson Laboratories, Inc. Corona, CA 92880 USA, NDC 0591-0825-01
Quantity: 10,615 bottles
Why Was This Recalled?
Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500 mg were found in a sealed 100 count bottle of Oxycodone and Acetaminophen Tablets, USP 10/650 mg lot# 705791A.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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