PlainRecalls
FDA Drug Moderate Class II Terminated

ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.

Reported: June 19, 2019 Initiated: May 31, 2019 #D-1341-2019

Product Description

ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.

Reason for Recall

Failed Dissolution Specifications: Out of specification result for dissolution.

Details

Recalling Firm
Chiesi USA, Inc.
Units Affected
2118 bottles
Distribution
Nationwide in the USA.
Location
Cary, NC

Frequently Asked Questions

What product was recalled?
ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.. Recalled by Chiesi USA, Inc.. Units affected: 2118 bottles.
Why was this product recalled?
Failed Dissolution Specifications: Out of specification result for dissolution.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 19, 2019. Severity: Moderate. Recall number: D-1341-2019.