4 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FLEXOR ANSEL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·July 20, 2017
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·November 7, 2008
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·September 1, 2011
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 17, 2013