19 results
·
55ms
·
Sources: EU EUDAMED, US FDA
BARDEX® FOLEY CATHETER SILICONE COATED
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·December 7, 2022
AMPLATZER VASCULAR PLUG
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code KRD·February 21, 2024
AMPLATZER VASCULAR PLUG
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code KRD·February 21, 2024
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·June 16, 2016
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·June 16, 2016
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·June 16, 2016
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·June 16, 2016
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·June 16, 2016
TORONTO (RETIRED)
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
EPIC¿ VALVE (AORTIC)
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
SJM TRIFECTA VALVE
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
TORONTO (RETIRED)
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
NAVITOR TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPT·October 29, 2025
NAVITOR TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code NPT·October 29, 2025
AMPLATZER PFO OCCLUDER
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code MLV·May 4, 2026
SJM TRIFECTA VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
EPIC¿ VALVE (AORTIC)
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code LWR·July 8, 2024
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Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices
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🇩🇪 Germany·464 Manufacturers·5263 Devices