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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Dr. Reddy's Glimepiride Tablets Recalled for Tablet Misprint

Agency Publication Date: February 6, 2024
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Summary

Dr. Reddy's Laboratories, Inc. has voluntarily recalled 73,761 bottles of Glimepiride (glimepiride) Tablets, USP 1mg, because of a misprint on the tablets. This recall involves 59,336 of the 100-count bottles and 14,425 of the 500-count bottles. The tablets are prescription medications used to treat type 2 diabetes and were distributed nationwide across the United States.

Risk

A misprint on a prescription tablet can cause patient confusion and could lead to medication errors, such as taking the wrong dose or the wrong medicine entirely. No injuries have been reported in connection with this misprint.

What You Should Do

  1. This recall affects Dr. Reddy's Glimepiride (glimepiride) 1mg Tablets sold in 100-count bottles (NDC 55111-320-01) and 500-count bottles (NDC 55111-320-05).
  2. To identify affected products, check the bottle label for lot numbers T2303622, T2303626, T2303627, T2303628, or T2303629 (100-count) or lots T2303609 or T2303610 (500-count), all with an expiration date of 06/2026.
  3. If you have health concerns about your medication, contact your healthcare provider or pharmacist immediately. Return any unused product to the place of purchase for a refund, throw it away, or contact Dr. Reddy's Laboratories, Inc. for further instructions.
  4. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Glimepiride Tablets, USP 1mg (100-count bottle)by Dr. Reddy's Laboratories Limited
Variants: 1mg, Tablet
Lot Numbers:
T2303622 (Exp. 06/2026)
T2303626 (Exp. 06/2026)
T2303627 (Exp. 06/2026)
T2303628 (Exp. 06/2026)
T2303629 (Exp. 06/2026)
NDC:
55111-320-01

Recall #: D-0312-2024; Quantity: 59,336 bottles

Product: Glimepiride Tablets, USP 1mg (500-count bottle)by Dr. Reddy's Laboratories Limited
Variants: 1mg, Tablet
Lot Numbers:
T2303609 (Exp. 06/2026)
T2303610 (Exp. 06/2026)
NDC:
55111-320-05

Recall #: D-0313-2024; Quantity: 14,425 bottles

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93833
Status: Active
Manufacturer: Dr. Reddy's Laboratories, Inc.
Sold By: Pharmacies
Manufactured In: India
Units Affected: 2 products (59,336 bottles; 14,425 bottles)
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.