3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LEAD MODEL 304
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·January 29, 2013
REPROCESSED ETHICON 5MM TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 14, 2010
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·July 14, 2014