Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due to Subpotent drug: Two lots of Oxycodone and Acetaminophen...
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 Capsules, USP 5mg/500 mg, packaged in a)100-count bottle (NDC 0591-0737-01), b) 500-count bottle (NDC 0591-0737-05), Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA92880.
Quantity: 1,260 bottles
Why Was This Recalled?
Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500 mg are being recalled due to low out of specification (OOS) assay result obtained at expiry (24 months) for the oxycodone portion of the product.
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