11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SEE H10
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·March 4, 2019
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·April 20, 2018
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·January 26, 2025
POWER SUPPLY
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code MRZ·September 14, 2016
POWER SUPPLY (FIXED HEADS )ASM
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code MRZ·May 23, 2016
ASR ACETABULAR CUP 62
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·March 12, 2013
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·February 18, 2011
MARLEX PATCH WITH BARD PERFIX PLUG
FDA Adverse Event
Injury
·C. R. BARD INC. / DAVOL INC.·Product code FTL·February 12, 2008
THORATEC® HEARTMATE 3¿ SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·March 4, 2024
FMS VUE PUMP
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·September 11, 2020
ADVANTA V12,COVERED STENTSYS, 9X59X120
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026