Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 mL, Single patient infusion vial, RX only, Hospira, Inc., L
Recalled August 21, 2013 · FDA recall D-887-2013 · Hospira
Hazard
Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection identified as stainless steel · FDA Class II
Units
94,110 vials
Sold at
Nationwide
Description
Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection identified as stainless steel
Product
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
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →