Class II
Terminated
Nalbuphine HCl Injection, 20 mg/mL, 10 mL Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1467-01
- Company
- Hospira Inc.
- Recall Initiated
- November 21, 2012
- Posted
- December 26, 2012
- Recall Number
- D-096-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 145,400 vials
- Firm Location
- Lake Forest, IL, United States
Reason for Recall
Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
Distribution
Nationwide and Puerto Rico.
Lot / Code Info
Lot #: 11-293-DK, Exp 05/01/13
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