4 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010
FDA Adverse Event
Malfunction
·SYNTHES OBERDORF·Product code HWE·July 10, 2017
TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWP·February 21, 2013
TECNIS CL
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·January 26, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014