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Class III: unlikely to cause harmOngoing

Dr. Reddy's Laboratories Glimepiride Tablets Recall

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class III
Reported by FDA
Feb 14, 2024
Recall ID
D-0312-2024
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Glimepiride Tablets starting Jan 18, 2024. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0312-2024 on Feb 14, 2024. Reason: Misprint on tablet. Status: Ongoing.

Why it was recalled

Misprint on tablet

Product description

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01

Lot numbers, UPCs & expiration codes

Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0312-2024
Classification
Class III
Status
Ongoing
Recall initiated
Jan 18, 2024
FDA report date
Feb 14, 2024
Quantity
59,336 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0312-2024, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Ongoing
Country
United States
Event ID
93833
Address
107 College Rd E
Code information
Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026
Postal code
08540-6623
Report date
Feb 14, 2024
Product type
Drugs
Recall number
D-0312-2024
Classification
Class III
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
59,336 bottles
Reason for recall
Misprint on tablet
Voluntary / mandated
Voluntary: Firm initiated
Product description
Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01
Distribution pattern
Nationwide
Recall initiation date
Jan 18, 2024
Initial firm notification
Letter
Center classification date
Feb 6, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0312-2024, published Feb 14, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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