3 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ADVIA CENTAUR XP RUBELLA G (RUB G) ASSAY
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LFX·April 24, 2014
JOURNEY KNEE IMPLANT
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·October 3, 2012
INFUSOR LV5, 12 PK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 27, 2010