Zydus Pharmaceuticals recalls Nelarabine injection due to failed impurities and degradation specifications. This medication, used for cancer treatment, may have unsafe levels of impurities that could cause harm.
Failed Impurities/Degradation Specifications
Zydus Pharmaceuticals is recalling Nelarabine injection (250mg/50mL) because it may contain impurities or degrade improperly. This could pose a risk to patients receiving the medication for cancer treatment.
The medication may contain impurities or degrade improperly, which could lead to unsafe levels of substances that might cause harm to patients. This is a serious concern for individuals receiving the drug for cancer treatment.
Patients prescribed Nelarabine injection for cancer treatment by a healthcare provider. Those using the medication without medical supervision are not affected.
Check for the product name 'Nelarabine Injection, 250mg/50mL' with NDC codes 70710-1726-1 or 70710-1726-8. The medication is only available by prescription and was manufactured by Zydus Lifesciences Ltd in India.
Inform your doctor or healthcare provider about the recall and ask if you have the recalled Nelarabine injection.
The recall indicates potential impurities or degradation, so it is not safe to use without consulting your healthcare provider.
Contact your healthcare provider to determine if you have the recalled product and follow their instructions.
Look for the NDC codes 70710-1726-1 or 70710-1726-8 on the packaging. This medication is only available by prescription.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0255-2025 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0255-2025 from Zydus Pharmaceuticals. 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.
