Reported Jun 20, 2012 · Terminated
Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured…
Endo Pharmaceuticals, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Endo Pharmaceuticals, Inc. · 100 Endo Blvd · Chadds Ford, PA · 19317
Is this the product you have?
- Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only
- Manufactured forEndo Pharmaceuticals Inc., Chadds Ford, PA
- ByNovartis, Lincoln, NE 68501; NDC 60951-797-70
- Lot codes and dates
Lot #: 402794NVExp 12/13
- Amount recalled
- 11,764 bottles
Where it was sold
- Nationwide
- PR
Why it was 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.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Endo Pharmaceuticals, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.