9 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
POSIFLUSH
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026
POSIFLUSH
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026
BD POSIFLUSH
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026
BD POSIFLUSH
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026
POSIFLUSH
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·April 6, 2026
ENDOPLEGE SINUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·November 26, 2008
OXFORD UNICOMPARTMENTAL KNEE FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET, INC.·Product code HRY·September 2, 2011
1722028-2013-01307
FDA Adverse Event
Malfunction
·GAMBRO BCT, INC.·July 29, 2013
LOGIC CR TIB INSERT SLOPE++, SZ 2, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 28, 2022