Amerisource Health Services recalls Glimepiride 1mg tablets due to FDA inspection findings. Products with specific NDC numbers and batch dates are affected.
CGMP Deviations: recalling drug products following an FDA inspection.
Amerisource Health Services is recalling Glimepiride 1mg tablets from specific bottle counts and batch numbers because of FDA inspection findings. This recall is necessary to ensure drug safety following regulatory issues.
The recall is due to FDA inspection findings indicating potential quality control issues during manufacturing. These deviations could affect the safety and effectiveness of the medication.
Prescription diabetes medication users who have the recalled Glimepiride tablets with the listed NDC numbers and batch dates are affected. People taking this medication should check their product details.
Check for Glimepiride Tablets, 1 mg, RX, in 100-count or 500-count bottles with specific NDC numbers and batch dates listed in the recall notice.
Identify the NDC number and batch date on your Glimepiride tablets to confirm if they are in the recalled list.
The FDA found quality control issues during manufacturing, so Amerisource Health Services is recalling these specific batches of Glimepiride tablets.
Check the NDC number and batch date on your tablets to see if they are in the recalled list. If they are, contact Amerisource Health Services for further instructions.
The recall is due to FDA inspection findings, but the official notice does not specify the exact safety risks or injuries associated with the product.
We’ve drafted a message you can send Amerisource Health Services to request your refund or repair — edit it as you like.
Subject: Recall D-0757-2023 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0757-2023 from Amerisource Health Services. 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.
