8 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 1, 2022
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 1, 2022
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 7, 2022
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 1, 2022
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 1, 2022
TRIMA ACCEL
FDA Adverse Event
Malfunction
·TERUMO BCT·Product code GKT·November 14, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013
BD DISCARDIT¿ II SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2018