Class II
Terminated
Morphine Sulfate Injection, USP, (25mg/mL), 250 mg, 10mL Fill, Single dosage Flip top Vial, (C-II), (NDC 0409-1135-02), Rx Only, Manfactured for Hospira, Inc., Lake Forest, IL 60045 USA.
This recall has been terminated (originally issued December 11, 2013).
- Company
- Hospira Inc.
- Recall Initiated
- September 16, 2013
- Posted
- December 11, 2013
- Recall Number
- D-023-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 29,700 vials
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Lack of Assurance of Sterility: Confirmed customer report of leakage of vial contents due to the breaking of the vial neck.
Distribution
Nationwide
Lot / Code Info
Lot #17368EV Exp 08/13
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