CLONIDINE TRANSDERMAL SYSTEM Recalls

3 recalls found for CLONIDINE TRANSDERMAL SYSTEM. Check if any of your products are affected.

Health & Personal Care

HIGH

FDA DRUG

Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)

Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.

Mar 19, 2026

CLONIDINE TRANSDERMAL SYSTEM

CGMP Deviations:

Health & Personal Care

HIGH

FDA DRUG

Teva Clonidine Transdermal System Recall Expands Over CGMP Deviations, 124,054 Cartons Affected (202

Teva Pharmaceuticals recalled 124,054 cartons of Clonidine Transdermal System due to CGMP deviations from an unapproved raw material. The recall affects products sold in the United States. Consumers should stop using the product immediately and consult a healthcare provider for guidance.

Mar 19, 2026

Clonidine Transdermal System

CGMP Deviations:

HIGH

FDA DRUG

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...

CGMP Deviations: use of an unapproved raw material

Mar 19, 2026

CLONIDINE TRANSDERMAL SYSTEM

CGMP Deviations:

Brand Statistics

Total Recalls

Pages

CLONIDINE TRANSDERMAL SYSTEM Recalls

Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)

Teva Clonidine Transdermal System Recall Expands Over CGMP Deviations, 124,054 Cartons Affected (202

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...

Brand Statistics

Related Brands