3 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 9, 2014
840 VENTILATOR
FDA Adverse Event
COVIDIEN, FORMERLY NELLCOR·Product code CBK·October 19, 2012
RADIOLUCENT DRIVE MARK II
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HWE·May 28, 2015