3 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TK TI-KNOT DEVICE
FDA Adverse Event
LSI SOLUTIONS, INC.·Product code GCJ·June 10, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 9, 2013
NC SPRINTER RX BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code LOX·November 2, 2010