7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
CELL-DYN SAPPHIRE VENT HEAD ASSEMBLY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·March 8, 2011
OXFORD UNI KNEE PHASE III 4.0MM DIAM. FEMORAL DRILL
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HTW·November 20, 2009
OXFORD MP 04MM DRILL
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code NRA·April 13, 2017
VARISOFT
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 22, 2025
OXFORD PH3 CEMENTLESS FEM SZ M
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code NRA·June 20, 2025