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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Dr. Reddy's Laboratories, Inc. 2024-02-14 Health moderate FDA
Health · FDA · Recall #FDA-D-0313-2024

Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's… Recall

Issued February 14, 2024 · Dr. Reddy's Laboratories, Inc.

In February 2024, Dr. Reddy's Laboratories, Inc. recalled the Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's…, a moderate health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Misprint on tablet

What you should do

  1. 1 Stop using Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Dr. Reddy's Laboratories, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Dr. Reddy's Laboratories, Inc.
Category
Health
Recall date
February 14, 2024
Units affected
Not reported
Sold at
Nationwide
Recall number
FDA-D-0313-2024
Made in
United States
Issuing agency
FDA

In context

  • Dr. Reddy's Laboratories, Inc. has 17 recalls in our database, including 3 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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