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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