Class II · Moderate risk
Nelarabine Injection
Failed Impurities/Degradation Specifications
Is Nelarabine recalled?
Yes — there is an active recall. 2 ongoing FDA recalls mention Nelarabine (3 total). Check the affected lots below.
Most common reason: Impurity / degradation (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Nelarabine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Nelarabine recalls on record
none so far in 2026; 3 on record, newest first
Class II · Moderate risk
Nelarabine Injection
Failed Impurities/Degradation Specifications
Class II · Moderate risk
Arranon (nelarabine)
Impurities/Degradation Products: Potential for drug related impurities to exceed the specification limits.
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