3,870 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PULSE GEN MODEL 103
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·August 12, 2021
LEAD MODEL 302
FDA Adverse Event
Injury
·LIVANOVA USA, INC.·Product code MUZ·May 2, 2019
LEAD MODEL 303
FDA Adverse Event
Injury
·LIVANOVA USA, INC.·Product code MUZ·December 8, 2025
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·January 23, 2014
VNS Therapy Programmer, Model 3000, v1.0 System
FDA Recall
Terminated
·Cyberonics, Inc·Product code MUZ·November 13, 2017
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·October 7, 2016
PROGRAMMING WAND
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·October 7, 2016
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·July 6, 2015
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code MUZ·July 31, 2015
LEAD MODEL 302
FDA Adverse Event
Injury
·CYBERONICS - HOUSTON·Product code MUZ·August 4, 2015
PULSE GEN MODEL 102
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code MUZ·July 20, 2015
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·July 17, 2015
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·February 15, 2012
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code MUZ·February 17, 2012
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS INC·Product code MUZ·February 23, 2012
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code MUZ·February 10, 2012
LEAD MODEL 302
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code MUZ·February 28, 2012
PULSE GEN MODEL 101
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code MUZ·February 6, 2012
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS INC·Product code MUZ·January 4, 2012
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code MUZ·February 29, 2012