9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 7, 2011
CLOSUREFAST CATHETER
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GEI·September 27, 2016
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·May 1, 2018
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·December 22, 2016
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 26, 2018
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 27, 2025