Reported Aug 21, 2013 · 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. · 275 N Field Dr · Lake Forest, IL · 60045-2579
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, NDC 0409-4699-24; Propofol Injectable Emulsion, 500 mg/50 mL, 50 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-33
- Lot codes and dates
Lot 07-950-DJ Exp. Date 1JUL201310-101-DJ Exp. Date 1OCT2013and 10-102-DJ Exp. Date 1OCT2013
- Amount recalled
- 94,110 vials
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection identified as stainless steel
This product could cause temporary or reversible health problems — stop using it.
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