11 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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M-1 COT - BASE HIGH LOAD 28
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 20, 2013
M-1 COT - BASE HIGH LOAD 28
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 18, 2013
SPINEASSIST SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·August 19, 2019
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
AUTOPLUSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·April 27, 2013
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 18, 2014
3002 SECURE II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 16, 2011
EDWARDS SAPIEN 3 ULTRA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·March 6, 2024
PIRANHA
FDA Adverse Event
Injury
·RICHARD WOLF GMBH·Product code JCX·January 5, 2022
EDWARDS SAPIEN 3 ULTRA RESILIA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 6, 2024