11 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
IMPELLA RP PUMP
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code OZD·February 6, 2020
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 30, 2023
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 10, 2023
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code LWS·October 3, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·May 31, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 25, 2011
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·March 5, 2013
EDWARDS SAPIEN 3 ULTRA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·March 6, 2024
BD Q-SYTE¿ EXTENSION SET MICRO BORE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 4, 2021
IMPELLA 5.0
FDA Adverse Event
Death
·ABIOMED INC.·Product code OZD·February 3, 2022
EDWARDS SAPIEN 3 ULTRA RESILIA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 6, 2024