Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL Single patient infusion vial, Rx only, Hospira, Inc., L
Recalled May 1, 2013 · FDA recall D-297-2013 · Hospira
Hazard
Presence of Particulate Matter: A single visible particulate was identified during a retain sample inspection. · FDA Class II
Units
245,250 vials
Sold at
Nationwide and Puerto Rico
Description
Presence of Particulate Matter: A single visible particulate was identified during a retain sample inspection.
Product
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.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →