8 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CT LUCIA
FDA Adverse Event
Injury
·CARL ZEISS MEDITEC PRODUCTION LLC·Product code HQL·November 19, 2025
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·May 13, 2013
SELOX ST 53
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVN·September 23, 2014
VASOVIEW HEMOPRO 2 EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·May 17, 2011
PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 18, 2013
CT LUCIA 602
FDA Adverse Event
Injury
·CARL ZEISS MEDITEC PRODUCTION LLC·Product code HQL·December 16, 2022
HI-FLOW T-CONN W/LL & 1 VLV PORT
FDA Adverse Event
Malfunction
·CFN MEXICO 215 SA DE CV·Product code FPA·July 9, 2020
PROMUS ELEMENT¿ PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 18, 2012