Class II Recall

Teva Pharmaceuticals USA, Inc

Product
Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc, Parsippany, NJ, NDC 0591-3509-04 carton, NDC 0591-3509-54 pouch
Reason
CGMP Deviations: use of an unapproved raw material
Classification
Class II
Status
Ongoing
Lot
Lot: 100060002, Exp.: 07/2026; 100066802, Exp.: 05/2027
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.