PlainRecalls
FDA Drug Low Class III Terminated

Oxecta(TM) (oxycodone HCl) tablets, 5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-525-01

Reported: March 11, 2015 Initiated: February 26, 2015 #D-0403-2015

Product Description

Oxecta(TM) (oxycodone HCl) tablets, 5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-525-01

Reason for Recall

Failed Impurities/Degradation Specifications

Details

Recalling Firm
Pfizer Inc.
Units Affected
137 bottles
Distribution
Nationwide
Location
New York, NY

Frequently Asked Questions

What product was recalled?
Oxecta(TM) (oxycodone HCl) tablets, 5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-525-01. Recalled by Pfizer Inc.. Units affected: 137 bottles.
Why was this product recalled?
Failed Impurities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on March 11, 2015. Severity: Low. Recall number: D-0403-2015.