Northwind Pharmaceuticals recalls 2mg Glimepiride Tablets with specific NDCs and lots due to CGMP deviations. Affected products may not meet quality standards.
CGMP Deviations
Northwind Pharmaceuticals is recalling 2mg Glimepiride Tablets in 30-count and 90-count bottles with specific NDC numbers and lot dates because of manufacturing quality issues. This recall is important because the products may not meet the required quality standards, potentially affecting safety.
CGMP deviations refer to failures in the manufacturing process that could result in products not meeting quality standards. This means the medication might not be safe or effective for patients.
People who have the specific 2mg Glimepiride Tablets with NDC numbers 51655-383-52 or 51655-383-26 and the listed lot numbers are affected. Those using prescription diabetes medication are most at risk.
Check for 2mg Glimepiride Tablets in 30-count bottles (NDC 51655-383-52) or 90-count bottles (NDC 51655-383-26). Look for specific lot numbers: F106252201, F106252301, F106252303 (expiring 09/30/2024 or 5/31/2025) or F106252304 (expiring 07/31/2025) for the 30-count bottles, and F106252302 (expiring 07/31/2025) for the 90-count bottles.
Identify the NDC number and lot numbers listed in the recall notice to confirm if your medication is affected.
The recall is due to CGMP deviations, which means the manufacturing process did not meet quality standards.
The official notice does not specify a remedy, so contact Northwind Pharmaceuticals for guidance.
Yes, check for lot numbers F106252201, F106252301, F106252303 (expiring 09/30/2024 or 5/31/2025) or F106252304 (expiring 07/31/2025) for 30-count bottles, and F106252302 (expiring 07/31/2025) for 90-count bottles.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0551-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0551-2023 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.
