PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: March 11, 2015 Initiated: February 26, 2015 #D-0404-2015

Product Description

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

Details

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

Frequently Asked Questions

What product was recalled?
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. Recalled by Pfizer Inc.. Units affected: 139 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-0404-2015.