Reported Sep 18, 2013 · Terminated
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), packaged in 5 Units x 20 mL Single patient infusion vials…
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. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- 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
- Lot codes and dates
Lot #: 24-461-DJ*Exp 12/1426-543-DJ*Exp 02/1527-555-DJ*27-559-DJ*Exp 03/15*lot number may be followed by 01
- Amount recalled
- 283,150 vials
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulate Matter: Visible particulate embedded in the glass vial was observed and confirmed in a sample bottle during retain sample inspection.
This product could cause temporary or reversible health problems — stop using it.
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