7 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CONTACT DETACH
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 5, 2025
REFORM 6.5 X 45MM POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·PRECISON SPINE, INC·Product code MNH·March 24, 2015
POLYAXIAL DRIVER, REFORM
FDA Adverse Event
Injury
·PRECISION SPINE, INC.·Product code HXX·March 24, 2015
POLYAXIAL DRIVER, REFORM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code HXX·March 24, 2015
HOHMANN STYLE ARM 183MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTD·February 28, 2013
UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code MZV·March 1, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 21, 2008