10 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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EXCELSIOR MICROCATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code DQY·April 13, 2010
EXCELSIOR MICROCATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code DQY·May 18, 2010
EXCELSIOR MICROCATHETER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - CORK·Product code DQY·August 2, 2010
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 12, 2014
QUICKFLEX XL LV LEAD
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2011
INDURA
FDA Adverse Event
Injury
·RICE CREEK MANUFACTURING·Product code LKK·March 14, 2008
FMS
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·April 27, 2026
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 19, 2023
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·January 19, 2023
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Death
·COVIDIEN MFG DC BOULDER·Product code GEI·January 20, 2023