Budesonide Extended-Release Tablets recall: Failed Dissolution
Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA, UPC 5140782430, NDC 51407-824-30
Why was Budesonide Extended-Release Tablets recalled?
Failed Dissolution Specifications
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: GS054862, Exp. Date 07/31/2025
- Product
- Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA, UPC 5140782430, NDC 51407-824-30
- Recalling firm
- Golden State Medical Supply Inc.
- Quantity
- 108 bottles
- Distribution
- Illinois only
- Recall date
- February 7, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)