HIGHFDA DRUG

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
April 27, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
April 27, 2026
Hazard Level
HIGH
Brands
PRIMIDONE, Golden State Medical Supply, Inc
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
PRIMIDONE, Golden State Medical Supply, Inc
Model numbers
Lot #: GS067909, Exp 4/30/2028, GS068646, Exp 8/31/2026
UPC codes
51407-637, 51407-638, 51407-637-01, 51407-637-05, 51407-638-01
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    April 27, 2026

  2. Reported by FDA DRUG

    May 27, 2026

  3. RecallRadar source check

    June 3, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Golden State Medical Supply Inc. or your healthcare provider for guidance. Notification method: Letter

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Full Description

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01. Generic: PRIMIDONE; Brand: PRIMIDONE. Reason: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.. Classification: Class III. Quantity: 1,620 bottles. Distribution: USA Nationwide

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot #: GS067909
Exp 4/30/2028
GS068646
Exp 8/31/2026
UPC Codes
51407-637
51407-638
51407-637-01
+2 more
Affected States
ALL
Report Date
May 27, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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