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

Glenmark Pharmaceuticals Inc., USA 2023-11-15 Health serious FDA
Health · FDA · Recall #FDA-D-0095-2024

Deferasirox Tablets for Oral Suspension, 500mg, 30-count bottle, Rx only, Manufactured… Recall

Issued November 15, 2023 · Glenmark Pharmaceuticals Inc., USA

In November 2023, Glenmark Pharmaceuticals Inc., USA recalled the Deferasirox Tablets for Oral Suspension, 500mg, 30-count bottle, Rx only, Manufactured…, 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

Failed Dissolution Specifications

What you should do

  1. 1 Stop using Deferasirox Tablets for Oral Suspension, 500mg, 30-count bottle, Rx only, Manufactured… 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
November 15, 2023
Units affected
Not reported
Sold at
USA nationwide
Recall number
FDA-D-0095-2024
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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