Reported Feb 4, 2015 · Terminated
Propofol Injectable Emulsion, 1%, 200 mg/20 mL, (10mg/mL), 20 mL, Single patient infusion vial, Contains Benzyl…
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%, 200 mg/20 mL, (10mg/mL), 20 mL, Single patient infusion vial, Contains Benzyl Alcohol, For I.V. Administration, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30
- Lot codes and dates
Lot 35-844-DJExp 11/01/2015
- Amount recalled
- 126,075 vials
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulate Matter: The firm received a complaint of an embedded particulate in the neck of one vial composed primarily of iron.
This product could cause temporary or reversible health problems — stop using it.
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