7 results
·
29ms
·
Sources: EU EUDAMED, US FDA
ENvue Medical (USA) Inc.
FDA registration
ENvue Medical (USA) Inc.·2 products·🇺🇸 United States
ID NOW COVID-19
FDA Adverse Event
Injury
·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·May 21, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 25, 2021
ENVUE® ENTERAL FEEDING TUBE WITH STYLET AND ENFIT® CONNECTOR
FDA Adverse Event
Malfunction
·ENVUE MEDICAL (USA) INC.·Product code KNT·June 5, 2025
ENVUE FEEDING TUBE PLACEMENT SYSTEM
FDA Adverse Event
Death
·ENVUE MEDICAL (USA) INC.·Product code KNT·March 13, 2026
Dengue IgM ELISA 96 Well Kit, Catalog Number: DE051M The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only.
FDA Recall
Terminated
·Calbiotech Inc·Product code NWY·August 27, 2008
Dengue IgG ELISA 96 Well Kit, Catalog Number: DE050G The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only. The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only.
FDA Recall
Terminated
·Calbiotech Inc·Product code NWY·August 27, 2008