4 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
CATHETER, OPEN END URETERAL AXXCESS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code EYB·June 10, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008
SPINE INSTRUMENTS
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·November 19, 2025