Reported Sep 5, 2012 · Terminated
Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 ml Single patient infusion vial, Rx only, Hospira, Inc.…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc. · 375 N Field Dr · Lake Forest, IL · 60045-2513
Is this the product you have?
- 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
- Lot codes and dates
07-893-DJexp. 7/201310-123-DJ10-125-DJexp. 10/2013
- Amount recalled
- 56,420 vials
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulate Matter: A single visible particulate was observed and confirmed in a sample bottle during retain inspection.
This product could cause temporary or reversible health problems — stop using it.
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