5 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ACCU-CHEK INFORM II INSTRUMENT WITH RF CARD
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·October 21, 2021
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·May 8, 2013
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014
UNIVERSAL STEM 75X14MM FLUTED
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·May 17, 2011
EVOLUT FX PLUS VALVE
FDA Adverse Event
Injury
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·August 27, 2025