Endo Pharmaceuticals has issued a voluntary nationwide consumer level recall of Endocet (oxycodone/acetaminophen) tablets, 10 mg / 325mg, in 100-count bottles, in the US.

The affected lots are numbers 402415NV and 402426NV, and NDC 60951-712-70.

The recalled bottles were found to contain some Endocet 10mg / 650 mg tablets, which are identifiable by their larger size, different shape and different markings.

The company said adverse reactions experienced with the use of the tablets may be reported to US Food and Drug Administration MedWatch Adverse Event Reporting programme.