Teva Pharmaceuticals Usa, Inc: Clonidine Transdermal System, Usp, 0.2 Mg/day, Supplied In Cartons Of 4 Systems And 4 Adhesive Covers

Recalling firm

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

Category

drug recall

Country

United States

Agency

U.S. Food and Drug Administration

Recall date

2026-03-19

Status

Ongoing

Distribution

Within U.S

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/b36f6395-ce97-4582-9e5a-58b62138bdbd