Glenmark Pharmaceuticals recalls 150mg Lacosamide tablets due to CGMP deviations. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 150mg Lacos: 60-count bottles that were manufactured with CGMP deviations. This recall is for prescription-only medication that may pose safety risks if used improperly.
CGMP deviations refer to manufacturing process issues that could affect the safety and quality of the medication. This may lead to potential risks if the tablets are not properly controlled or stored.
Prescription holders of Lacosamide 150mg tablets with specific lot numbers and expiration dates. Patients using these tablets for seizure treatment are most at risk.
Check for lot numbers 17241125 with expiration dates June 26, 2026, November 26, 2026, or December 26, 2026. The product is a prescription-only 150mg Lacosamide tablet bottle.
Verify the lot number and expiration date on the bottle to confirm if it is affected.
The recall is due to CGMP deviations, which may affect safety. The manufacturer recommends checking the product details before use.
The recall record does not specify a replacement process or remedy.
The recall record does not provide specific instructions for affected products.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0343-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0343-2025 from Glenmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
