4 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·October 3, 2012
PLM A+ SPANISH 110V
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 18, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code NBW·August 27, 2007
MICRA
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DYB·February 21, 2020