Drug recall D-1672-2012
Product
Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 ml Single patient infusion vial, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-4699-24
Reason for recall
Presence of Particulate Matter: A single visible particulate was observed and confirmed in a sample bottle during retain inspection.
Lots and codes
07-893-DJ, exp. 7/2013, 10-123-DJ, 10-125-DJ, exp. 10/2013
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 56,420 vials
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 3, 2012
- Terminated
- May 6, 2014
Related products
- Propofol – drug information
- NDC 0409-0010 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-4699 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-0501 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-6010 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-1511 Propofol · Propofol 10 mg/mL · Hospira, Inc.