FDAFDA · Food and drugs·Recall number D-1381-2012
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.
Published June 20, 2012 · Recall initiated: May 7, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Endo Pharmaceuticals, Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot #: 402794NV, Exp 12/13
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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