11 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·February 13, 2026
COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH CONTOUR ADVANCE® ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·February 13, 2026
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·May 24, 2013
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code PFO·January 15, 2024
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PGQ·July 4, 2016
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code PGQ·August 1, 2016
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·February 20, 2013
POWERHEART G3 PLUS AED
FDA Adverse Event
Death
·CARDIAC SCIENCE CORPORATION·Product code MKJ·January 13, 2011
KEYLESS DRIVER
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBE·December 11, 2013
PREPSTAIN SLIDE PROCESSOR
FDA Adverse Event
Injury
·TRIPATH IMAGING·Product code KPA·March 17, 2010
BD TOTALYS SLIDEPREP
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MKQ·February 28, 2025