Recall
FDAHealthMarch 19, 2026

Teva Pharmaceuticals USA, Inc — Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx Only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake

⚠️ CGMP Deviations: use of an unapproved raw material

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
March 19, 2026

Within U.S

What's affected?

Product
Clonidine Transdermal System, USP, 0.1 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 0591-3508-04 carton, NDC 0591-3508-54 pouch
Lot code
100060315

Additional details

Lot: 100060315, Exp.: 04/2026; 100068644, Exp.: 01/2027.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 124,054 Cartons.

View original FDA notice →

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