Teva Pharmaceuticals USA, Inc 2024-02-07 Health serious FDA
Health · FDA · Recall #FDA-D-0275-2024
Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by:… Recall
Issued February 7, 2024 · Teva Pharmaceuticals USA, Inc
In February 2024, Teva Pharmaceuticals USA, Inc recalled the Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by:…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Dissolution Specifications
What you should do
- 1 Stop using Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by:… 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
- February 7, 2024
- Units affected
- Not reported
- Sold at
- Nationwide
- Recall number
- FDA-D-0275-2024
- 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 737th Health recall we've logged in 2024.