4 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
1628664-2017-00360
FDA Adverse Event
Malfunction
·September 27, 2017
MITEK VAPR S90 SUCTION ELECTRODE W/INTEGRATED HANDPIECE
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code GEI·May 9, 2014
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 29, 2010
PRECISION XTRA /OPTIUM
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·August 31, 2007