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Serious recall: Injury is possible or has been reported. Take action promptly.

Glenmark Pharmaceuticals Inc., USA 2023-12-06 Health serious FDA
Health · FDA · Recall #FDA-D-0124-2024

Naproxen Tablets, USP 250mg, 100-count bottle, Rx Only, Manufactured by: Glenmark… Recall

Issued December 6, 2023 · Glenmark Pharmaceuticals Inc., USA

In December 2023, Glenmark Pharmaceuticals Inc., USA recalled the Naproxen Tablets, USP 250mg, 100-count bottle, Rx Only, Manufactured by: Glenmark…, a serious 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

Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

What you should do

  1. 1 Stop using Naproxen Tablets, USP 250mg, 100-count bottle, Rx Only, Manufactured by: Glenmark… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Glenmark Pharmaceuticals Inc., USA 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
Glenmark Pharmaceuticals Inc., USA
Category
Health
Recall date
December 6, 2023
Units affected
Not reported
Sold at
Nationwide
Recall number
FDA-D-0124-2024
Made in
United States
Issuing agency
FDA

In context

  • Glenmark Pharmaceuticals Inc., USA has 53 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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