FDA recall D-0404-2015

Pfizer Inc. · Class III · drug

Product

Oxecta(TM) (oxycodone HCl) tablets, 7.5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-526-01

Reason for recall

Failed Impurities/Degradation Specifications

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2015-02-26
Report date: 2015-03-11
Termination date: 2017-07-29
Voluntary/Mandated: Voluntary: Firm initiated
Location: New York, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0404-2015