RecallDepth
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.

This recall has been terminated (originally issued June 20, 2012).

Company
Endo Pharmaceuticals, Inc.
Recall Initiated
May 7, 2012
Posted
June 20, 2012
Recall Number
D-1381-2012
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
11,764 bottles
Firm Location
Chadds Ford, PA, United States
Official Source
View on FDA website ↗

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.

Distribution

Nationwide and Puerto Rico

Lot / Code Info

Lot #: 402794NV, Exp 12/13

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