Reported May 1, 2013 · Terminated
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 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. · 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), 20 mL Single patient infusion vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30.
- Lot codes and dates
Lot #: 11-185-DJ*11-196-DJ*Exp 1NOV2013* may be followed by 01 or 02
- Amount recalled
- 245,250 vials
Where it was sold
- Nationwide
- PR
Why it was recalled
Presence of Particulate Matter: A single visible particulate was identified during a retain sample inspection.
This product could cause temporary or reversible health problems — stop using it.
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