PlainRecalls
FDA Drug Low Class III Terminated

Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 0591-3508-04

Reported: November 24, 2021 Initiated: October 28, 2021 #D-0235-2022

Product Description

Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 0591-3508-04

Reason for Recall

Failed Impurities/Degradation Specifications

Details

Recalling Firm
Teva Pharmaceuticals USA
Units Affected
64,978 patches
Distribution
Nationwide and Puerto Rico
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 0591-3508-04. Recalled by Teva Pharmaceuticals USA. Units affected: 64,978 patches.
Why was this product recalled?
Failed Impurities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on November 24, 2021. Severity: Low. Recall number: D-0235-2022.