4 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNI LFIT MEDIAL FEMORAL COMP.
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 13, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
UNKNOWN BLADE
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS CORK·Product code HAB·November 23, 2010