Hospira Inc.: Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL),
Recall reason: Failed Impurities/Degradation Specifications: Out of Specification(OOS) results for degradation product of etomidate was confirmed during stability testing.. Recalled by Hospira Inc.. Distribution: Nationwide. Classification (Class III — minor violation). Affected lots/NDC/dates: Lot 34-531-DK, Exp 10/01/2015. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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