Glenmark recalls 500mg Deferasirox oral suspension tablets due to failed dissolution specifications. Affected lots from 2022-2024 may not dissolve properly, risking ineffective treatment. Stop using and contact for return.
Failed Dissolution Specifications
Glenmark is recalling 500mg Deferasirox oral suspension tablets that may not dissolve properly. This could lead to ineffective treatment for patients with iron overload conditions. Affected products were sold with specific lot numbers and expiration dates.
The tablets may not dissolve properly in the mouth, which could lead to ineffective treatment. This is a quality issue with the dissolution specifications, not a safety hazard like choking or injury.
Patients prescribed Deferasirox tablets for iron overload conditions who have the specific lot numbers listed. Those with the product from the listed expiration dates are most at risk.
Check the product label for the lot numbers: 17220063 (exp 12/2023), 17220396/17220397 (exp 01/2024), 17220965 (exp 04/2024), 17221187/17221523 (exp 07/2024), 17221793/17221794/17221801 (exp 08/2024).
Look for the lot numbers listed in the recall notice to confirm if your product is affected.
Reach out to Glenmark Pharmaceuticals for instructions on returning the product or getting a replacement.
The recall is due to failed dissolution specifications, which may lead to ineffective treatment. The product is not safe for use as intended.
Contact Glenmark Pharmaceuticals directly for instructions on returning the product or getting a replacement.
Check the product label for the specific lot numbers listed in the recall notice: 17220063 (exp 12/2023), 17220396/17220397 (exp 01/2024), etc.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0095-2024 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0095-2024 from Glenmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
