Dr. Reddy's recalls 100-count Glimepiride tablets (1mg) due to a misprint on the tablets, which could lead to incorrect dosing. Affected lots were manufactured in India with specific expiration dates.
Misprint on tablet
Dr. Reddy's is recalling 100-count Glimepiride tablets (1mg) because of a misprint that might cause incorrect dosing. This could lead to unsafe medication levels if taken without proper guidance.
The misprint on the tablets could lead to incorrect dosing if the medication is taken without proper guidance. This might result in unsafe medication levels for people managing diabetes.
People who have the 100-count Glimepiride tablets (1mg) from Dr. Reddy's Laboratories in India with specific lot numbers and expiration dates are affected. Those taking diabetes medication are most at risk.
Check for the product name 'Glimepiride Tablets, USP 1mg, 100-count bottles' with the lot numbers T2303622 through T2303629 and expiration dates of 06/2026.
Look for the lot numbers T2303622 through T2303629 and expiration dates of 06/2026 on the packaging.
The recall record states there is a misprint on the tablets, but does not specify what the misprint is.
Check for the lot numbers T2303622 through T2303629 and expiration dates of 06/2026 on the packaging.
The recall does not specify a remedy, so there is no instruction to stop using the tablets.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0312-2024 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0312-2024 from Dr. Reddy's. 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.
