10 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HELICAL BLADE COUPLING SCREW
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·August 22, 2017
CUP: MPACT ACETABULAR SHELL Ø56 NO-HOLE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·July 15, 2022
VENATECH LP
FDA Adverse Event
Injury
·B.BRAUN MEDICAL SAS·Product code DTK·January 24, 2020
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
COULTER AC*T 5 DIFF AUTOLOADER (AL) ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·March 19, 2013
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·March 2, 2011
AXIUM 3D
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·June 9, 2025
AXIUM 3D
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code KRD·October 15, 2025
EXACTECH
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code LXH·October 28, 2021
HELICAL BLADE COUPLING SCREW
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·July 25, 2016