FDA Drugs recall ·
Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only… recall
- Recall number
- D-0235-2026
- Date
- (initiated November 26, 2025)
- Company / brand
- Golden State Medical Supply Inc.
5187 Camino Ruiz, Camarillo, CA, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 2472 HDPE Bottles
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10
Why was it recalled?
Presence of Foreign Tablets/Capsules
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot GS065762
Distribution
Nationwide within the USA
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0235-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.