8 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V·Product code FPA·December 30, 2025
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V·Product code FPA·December 30, 2025
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V·Product code FPA·December 30, 2025
SCORPIO PS TIB INSERT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·April 21, 2014
LOCKING BOLT MEASURING DEVICE F/TROCHANTERIC FIXATION NAILS
FDA Adverse Event
Malfunction
·SYNTHES JENNERSVILLE·Product code HTJ·December 5, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 6, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 10, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·March 12, 2008