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Class II: temporary or reversible health riskOngoing

Golden State Medical Supply Baclofen Tablets Recall

Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporat…

Golden State Medical Supply Inc. · Camarillo, CA

Risk level
Class II
Reported by FDA
Dec 24, 2025
Recall ID
D-0235-2026
Check your lot numberHow we source this data

Summary

Golden State Medical Supply recalled Baclofen Tablets starting Nov 26, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0235-2026 on Dec 24, 2025. Reason: Presence of Foreign Tablets/Capsules. Status: Ongoing.

Why it was recalled

Presence of Foreign Tablets/Capsules

Product description

Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10

Lot numbers, UPCs & expiration codes

Lot GS065762

Where it was sold

Nationwide within the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0235-2026
Classification
Class II
Status
Ongoing
Recall initiated
Nov 26, 2025
FDA report date
Dec 24, 2025
Quantity
2472 HDPE Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Golden State Medical Supply Inc.

Original FDA data

Every field from FDA enforcement report D-0235-2026, exactly as published.

Show all FDA fields
City
Camarillo
State
CA
Status
Ongoing
Country
United States
Event ID
98059
Address
5187 Camino Ruiz
Code information
Lot GS065762
Postal code
93012-8601
Report date
Dec 24, 2025
Product type
Drugs
Recall number
D-0235-2026
Classification
Class II
Recalling firm
Golden State Medical Supply Inc.
Product quantity
2472 HDPE Bottles
Reason for recall
Presence of Foreign Tablets/Capsules
Voluntary / mandated
Voluntary: Firm initiated
Product description
Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10
Distribution pattern
Nationwide within the USA
Recall initiation date
Nov 26, 2025
Initial firm notification
Letter
Center classification date
Dec 15, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0235-2026, published Dec 24, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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