RecallDepth
Class II Terminated

Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05

Company
Hospira Inc.
Recall Initiated
August 20, 2015
Posted
September 23, 2015
Recall Number
D-0418-2015
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
83,320 vials
Firm Location
Lake Forest, IL, United States

Reason for Recall

Defective Container: There were customer complaints of cracked and leaking glass vials.

Distribution

Nationwide

Lot / Code Info

Lot #s: 43406DD, Exp 7/1/2016; 44255DD, Exp 8/1/2016

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