RECALL: Endo Pharmaceuticals Recalls Endocet Tablets

Endo Pharmaceuticals issued a voluntary nationwide consumer level recall of Endocet (oxycodone/acetaminophen, USP) Tablets. One bottle from each lot of Endocet 10mg/325mg tablets, 100 count bottles, was found to contain some Endocet 10mg/650mg tablets, which are identifiable by their larger size, and different shape and markings. Currently, no other bottles from the subject lots or any other lots have been found to erroneously contain Endocet 10mg/650mg tablets.

The recall includes the following lots of this product:

  • Endocet (oxycodone/acetaminophen, USP) Tablets, 10mg/325mg 100 count bottles, NDC 60951-712-70, Lot # 402415NV, Expiry 01/2014; and
  • Endocet (oxycodone/acetaminophen, USP) Tablets, 10mg/325mg 100 count bottles, NDC 60951-712-70,Lot # 402426NV, Expiry 01/2014

For more information call (800) 462-ENDO or visit www.endo.com.