Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Endocet (oxycodone and acetaminophen) tablets Recalled by Endo Pharmaceuticals, Inc. Due to Adulterated Presence of Foreign Tablets: Customer complaint that...
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 Endo Pharmaceuticals, Inc. directly.
Affected Products
Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE 68501; NDC 60951-797-70.
Quantity: 11,764 bottles
Why Was This Recalled?
Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10 mg/650 mg tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Endo Pharmaceuticals, Inc.
Endo Pharmaceuticals, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report