Assurance Infusion recalls BUP 5.3MG/ FENT 1050 MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
Recalled January 22, 2020 · FDA recall D-0711-2020 · Assurance Infusion
Hazard
Lack of sterility assurance. · FDA Class II
Units
1 syringe
Sold at
Nationwide within the United States
Description
Lack of sterility assurance.
Product
BUP 5.3MG/ FENT 1050 MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
Manufacturer(s)
Assurance Infusion
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →