8 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
GRAFTON DBM
FDA Adverse Event
Injury
·MEDTRONIC EATONTOWN·Product code NUN·July 6, 2019
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 11, 2013
ONE TOUCH ULTRA LINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·May 22, 2008
SECURA DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWS·April 12, 2011
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 14, 2020
AMPLATZER TORQVUE 45X45 DELIVERY SHEATH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code DQY·February 11, 2025
EVOLUT FX PLUS VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 6, 2025
AMPLATZER AMULET
FDA Adverse Event
Death
·ABBOTT MEDICAL·Product code NGV·February 11, 2025