Recall RadarClonidine 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 8…
CGMP Deviations: use of an unapproved raw material
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Teva Pharmaceuticals USA, Inc — Parsippany, NJ
- Severity
- Class II — moderate
- Reported
- April 15, 2026
- Quantity
- 124,054 Cartons
- Recall number
- D-0472-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Within U.S
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