6 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
DRIVER SHAFT, T10 HEXALOBE, CANNULATED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·April 7, 2021
DRIVER SHAFT, T10 HEXALOBE, CANNULATED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 12, 2023
DRIVER SHAFT, T10 HEXALOBE, CANNULATED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 15, 2025
DRV SFT,T8 HEXALOBE CANN,STR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 12, 2023
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 19, 2010
PROMUS ELEMENT ¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 14, 2012