Assurance Infusion recalls BUP 35MG/FENT 1.5MG/ML in 20 mL syringe Assurance Infusion (713) 533-8800
Recalled January 22, 2020 · FDA recall D-0703-2020 · 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 35MG/FENT 1.5MG/ML 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 →