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
- Recalling Firm
- Endo Pharmaceuticals, Inc.
- 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.
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