308 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code QNR·March 30, 2026
ROTAFLOW 2-PUMPS CONSOLE
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTQ·May 28, 2015
CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026
CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026
CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026
CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code QNR·March 30, 2026
A.M.G. PMP PEDIATRIC STE CA
FDA Adverse Event
Injury
·EUROSETS S.R.L.·Product code DTZ·March 30, 2026
A.M.G. PMP PEDIATRIC STE CA
FDA Adverse Event
Injury
·EUROSETS S.R.L.·Product code DTZ·March 26, 2026
CENTRIMAG BLOOD PUMP, CAN
FDA Adverse Event
Injury
·THORATEC SWITZERLAND GMBH·Product code KFM·March 26, 2026
HLM TUBING SET W/BIOLINE COATING
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 24, 2015
QUADROX-ID AD.O.FIL.
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·December 9, 2014
HLS SET ADVANCED 7.0
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·November 24, 2020
HLS SET ADVANCED 7.0
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·November 4, 2020
CUSTOM TUBING PACK
FDA Adverse Event
Injury
·DATASCOPE CORP·Product code DTL·July 28, 2015
QUADROX-ID
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·October 17, 2014
UNKNOWN DISTRIBUTED DIALYZER
FDA Adverse Event
Injury
·*·Product code FJI·April 24, 1996
EVOKE SCS SYSTEM
FDA Adverse Event
Injury
·SALUDA MEDICAL PTY LTD·Product code LGW·October 10, 2023
UNKNOWN DISTRIBUTED DIALYZER
FDA Adverse Event
Injury
·*·Product code FJI·April 24, 1996
UNKNOWN DISTRIBUTED DIALYZER
FDA Adverse Event
Injury
·*·Product code FJI·April 24, 1996
TERUMO TAF175 (HF/CR/1.75/M)
FDA Adverse Event
Injury
·TERUMO CORP·Product code FJI·April 24, 1996