14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CARDIOSAVE HYBRID, 3.1 EDITION
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·November 14, 2023
PREMIUM PLUS CEEA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·April 19, 2018
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·July 22, 2024
CARDIOSAVE HYBRID, 3.1 EDITION
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·February 15, 2024
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·March 17, 2023
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MKJ·August 12, 2025
DRIVER SHAFT, T-15, SHORT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 18, 2025
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·March 13, 2013
OXFORD UNICOMPARTMENTAL KNEE PHASE 3 RIGHT MEDIAL TIBIAL TRAY STD SZ C
FDA Adverse Event
Injury
·BIOMET UK LTD·Product code NRA·February 25, 2011
PULMONETIC
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 203/PULMONETIC SYSTEMS, INC.·Product code CBK·February 25, 2008
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·July 31, 2025
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·February 2, 2023
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·October 18, 2024
CARDIOSAVE HYBRID, 3.1 EDITION
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·January 15, 2025