11 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Death
·COOK INC·Product code MIH·February 26, 2019
ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025
STOCKERT S3 GAS BLENDER
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014
GLUCOMMANDER, G+
FDA Adverse Event
Malfunction
·GLYTEC, LLC·Product code NDC·April 30, 2013
FORCETRIAD ENERGY PLATFORM
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code GEI·September 19, 2014
SETROX S 53
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO·Product code DTB·August 5, 2008
S3 GAS BLENDER SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017
S3 GAS BLENDER SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017
S3 ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·December 19, 2024
SORIN S3 GAS BLENDER
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTX·February 25, 2015
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Malfunction
·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·April 13, 2022