Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL single patient infusion vial packaged in 5 Units x 20 m
Recalled November 13, 2013 · FDA recall D-66637-001 · Hospira
Hazard
Presence of Particulate Matter: Visible particles embedded in the glass identified during a retain sample inspection. · FDA Class II
Units
70,450 vials
Sold at
Nationwide
Description
Presence of Particulate Matter: Visible particles embedded in the glass identified during a retain sample inspection.
Product
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL single patient infusion vial packaged in 5 Units x 20 mL per carton, 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 →