PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: June 20, 2012 Initiated: May 7, 2012 #D-1381-2012

Product Description

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.

Reason for Recall

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.

Details

Units Affected
11,764 bottles
Distribution
Nationwide and Puerto Rico
Location
Chadds Ford, PA

Frequently Asked Questions

What product was recalled?
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.. Recalled by Endo Pharmaceuticals, Inc.. Units affected: 11,764 bottles.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 20, 2012. Severity: Low. Recall number: D-1381-2012.