8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ARCHITECT I2000 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code NIG·August 21, 2013
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 22, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVAMEX·Product code FSA·November 5, 2012
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·May 1, 2018
STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 30, 2025
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·December 22, 2016
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·March 14, 2023
STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 17, 2025