10 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 18, 2013
PROMUS ELEMENT¿ PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 18, 2012
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·September 4, 2019
BD PHASEAL INJECTOR LUER LOCK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·August 3, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2022
RESOLUTE INTEGRITY RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·January 20, 2018
BD PHASEAL¿ INJECTOR LUER LOCK N35J
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·October 26, 2022
CONNECTION SHIELD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDJ·May 13, 2013
LINOX S 65
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·September 23, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN BENNETT CORP.·Product code CBK·April 28, 2011