D-0473-2026Class II

Teva Pharmaceuticals USA, Inc

Recalling firm

Product type

Drug

Status

Ongoing

Report date

2026-04-15

Distribution

Within U.S

Firm state

Product quantity

62,136 Cartons

Initiated by

Voluntary: Firm initiated

SPEQ quality domain

Documentation & Change Control

Reason for recall

CGMP Deviations: use of an unapproved raw material

Product description

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

Code / lot info

Lot: 100060002, Exp.: 07/2026; 100066802, Exp.: 05/2027

Other recalls SPEQ maps to Documentation & Change Control

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See all Documentation & Change Control recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.