3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·November 4, 2010
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·February 6, 2014
SEQUOIA NON-CANNULATED BONE TAP 6.5MM
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code KWQ·December 27, 2012