Sanofi-Aventis U.S. LLC: Elitek (rasburicase) for injection, 7.5 mg vial
Recall reason: Failed Stability Specifications: Out of Specification result for enzyme activity levels noted during routine stability testing.. Recalled by Sanofi-Aventis U.S. LLC. Distribution: Nationwide in the US. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot #: A9306, Exp 2/28/2022. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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