⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Teva Pharmaceuticals USA, Inc: Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Lab

DrugsSource: FDA (drug) · Date: 2026-04-15

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The text below is copied from the official FDA (drug) record. If anything differs, the official notice is correct.

Company / brand
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 / hazard
CGMP Deviations: use of an unapproved raw material
Classification
Class II
Status
Ongoing
Distribution / sold at
Within U.S
Recall initiated
2026-03-19
Code info
Lot: 100060002, Exp.: 07/2026; 100066802, Exp.: 05/2027
Product quantity
62,136 Cartons
Voluntary mandated
Voluntary: Firm initiated
City
Parsippany
State
NJ
Country
United States
Event id
98614
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