Teva Pharmaceuticals USA, Inc 2026-04-15 Health serious FDA
Health · FDA · Recall #FDA-D-0473-2026
Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4… Recall
Issued April 15, 2026 · Teva Pharmaceuticals USA, Inc
In April 2026, Teva Pharmaceuticals USA, Inc recalled the Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
CGMP Deviations: use of an unapproved raw material
What you should do
- 1 Stop using Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Teva Pharmaceuticals USA, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Teva Pharmaceuticals USA, Inc
- Category
- Health
- Recall date
- April 15, 2026
- Units affected
- Not reported
- Sold at
- Within U.S
- Recall number
- FDA-D-0473-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Teva Pharmaceuticals USA, Inc has 13 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.