Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 ml Single patient infusion vial, Rx only, Hospira, Inc. Lak
Recalled September 5, 2012 · FDA recall D-1672-2012 · Hospira
Hazard
Presence of Particulate Matter: A single visible particulate was observed and confirmed in a sample bottle during retain inspection. · FDA Class II
Units
56,420 vials
Sold at
Nationwide
Description
Presence of Particulate Matter: A single visible particulate was observed and confirmed in a sample bottle during retain inspection.
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 USA, NDC 0409-4699-24
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →