Assurance Infusion recalls QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
Recalled January 22, 2020 · FDA recall D-0764-2020 · Assurance Infusion
Hazard
Lack of sterility assurance. · FDA Class II
Units
190 vials
Sold at
Nationwide within the United States
Description
Lack of sterility assurance.
Product
QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
Manufacturer(s)
Assurance Infusion
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →