FDAFDA · Food and drugs·Recall number D-0095-2024
Deferasirox Tablets for Oral Suspension, 500mg, 30-count bottle, Rx only, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-496-30
Published November 15, 2023 · Recall initiated: October 20, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Dissolution Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DEFERASIROX
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Distributor
- USA nationwide
- Lot
- Lot #: 17220063, Exp 12/2023; 17220396, 17220397, Exp 01/2024; 17220965, Exp 04/2024; 17221187, 17221523, Exp 07/2024; 17221793, 17221794, 17221801, Exp 08/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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