Northwind Pharmaceuticals recalls 4mg Glimepiride tablets due to CGMP deviations. Affected lots expire 02/28/2025 or 09/30/2024. No remedy specified in recall notice.
CGMP Deviations
Northwind Pharmaceuticals is recalling 4mg Glimepiride tablets from specific lots because of manufacturing quality control issues. This recall is for patients who have these exact bottle sizes and lot numbers, as the tablets may not meet safety standards.
CGMP deviations mean the manufacturing process did not follow proper quality control standards. This could result in tablets that don't meet safety and effectiveness requirements, potentially causing issues for patients using them.
People who have the 30-count or 90-count bottles of Glimepiride 4mg tablets with the listed lot numbers and expiration dates are affected. Those taking this medication for diabetes are most at risk.
Check for 30-count bottles (NDC 51655-120-52) or 90-count bottles (NDC 51655-120-26) with lot numbers F105692201, F105692202, or F105692203. The expiration dates are 09/30/2024 or 02/28/2025.
Identify the bottle size, lot number, and expiration date to confirm if your tablets are affected.
The recall is due to CGMP deviations, which means the manufacturing process did not meet quality control standards.
The recall notice does not specify a remedy, so you should check the product details to see if your tablets are affected.
The recall notice does not provide a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0552-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0552-2023 from Northwind Pharmaceuticals. 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.
