Class II
Terminated
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), packaged in 5 Units x 20 mL Single patient infusion vials per carton, Rx only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-4699-30
This recall has been terminated (originally issued September 18, 2013).
- Company
- Hospira Inc.
- Recall Initiated
- August 14, 2013
- Posted
- September 18, 2013
- Recall Number
- D-932-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 283,150 vials
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter: Visible particulate embedded in the glass vial was observed and confirmed in a sample bottle during retain sample inspection.
Distribution
Nationwide
Lot / Code Info
Lot #: 24-461-DJ*, Exp 12/14; 26-543-DJ*, Exp 02/15; 27-555-DJ*, 27-559-DJ*, Exp 03/15; *lot number may be followed by 01
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