10 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 29, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 29, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 29, 2024
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·August 21, 2012
ARTERIAL PRESSURE MONITORING TRAY
FDA Adverse Event
Malfunction
·COOK INC·Product code DQO·December 3, 2024
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 20, 2013
GREENLIGHT MOXY
FDA Adverse Event
Malfunction
·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·July 7, 2011
PRINARY TUBING SET WITH 2 CLAVES
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·September 23, 2008
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 29, 2024
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 9, 2014