RecallDepth
Class III Ongoing

Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-8060-29

Company
Hospira Inc.
Recall Initiated
September 29, 2015
Posted
October 28, 2015
Recall Number
D-0054-2016
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
24,100 Syringes
Firm Location
Lake Forest, IL, United States

Reason for Recall

Failed Impurities/Degradation Specifications: Out of Specification(OOS) results for degradation product of etomidate was confirmed during stability testing.

Distribution

Nationwide

Lot / Code Info

Lot 34-531-DK, Exp 10/01/2015

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