D-0235-2022 Class III Terminated

Recalled by Teva Pharmaceuticals USA — Parsippany, NJ

Recall Details

Product Type
Drugs
Report Date
November 24, 2021
Initiation Date
October 28, 2021
Termination Date
February 27, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
64,978 patches

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

Distribution Pattern

Nationwide and Puerto Rico

Code Information

Lot# 1369117B, exp. date 11/2021