US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 12, 2024 (3 years ago)

Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Dissolution Specifications

What was recalled

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.
NDC code
51407-824-30
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0276-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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