8 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TARGETING ARM PROX. LAT TIBIA LEFT
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·February 2, 2012
INDIGO SYSTEM ASPIRATION CATHETER
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code QEW·August 7, 2023
DELTA CERAMIC FEM HD 36/+3MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 9, 2018
VOLUME VENTILATOR
FDA Adverse Event
Malfunction
·NELLCOR PURITAN BENNETT·Product code CBK·November 19, 2008
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011
OPTIFLUX F18NRE DIALYZER FINISHED ASSY
FDA Adverse Event
Injury
·OGDEN MFG.·Product code FJI·July 19, 2013
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·February 22, 2019
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·September 5, 2017