Glenmark Pharmaceuticals recalls 200mg Lacosamide tablets due to manufacturing deviations. Affected lots expire April 2025. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 200mg Lacosamide tablets that were manufactured with CGMP deviations. This recall affects specific lots that expire by April 2025. The issue means the product may not meet safety standards, so affected consumers should contact the company for instructions.
CGMP deviations refer to failures in the manufacturing process that could affect product safety and quality. These deviations might mean the tablets do not meet the required standards for safe use. However, the exact nature of the deviation is not specified in the recall notice.
People with prescriptions for Lacosamide tablets who purchased the recalled lots from pharmacies or hospitals. Those with specific lot numbers and expiration dates are most at risk.
Check the product label for the lot number and expiration date. The recalled items have specific lot numbers and expire by April 2025. The product is a prescription-only 200mg Lacosamide tablet bottle.
Look for the lot number and expiration date on the tablet bottle label.
The recall is due to CGMP deviations in manufacturing, which may affect product safety and quality. The exact nature of the deviation is not specified in the notice.
Check the product label for the lot number and expiration date. The recalled items have specific lot numbers that expire by April 2025.
Contact Glenmark Pharmaceuticals for instructions on what to do with the product. The recall notice does not specify a remedy.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0321-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0321-2025 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.
