4 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ANTHREX GUIDE WIRE; 1.1MM AR 8737-41
FDA Adverse Event
Malfunction
·ANTHREX, INC.·Product code HWC·August 23, 2021
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 19, 2010
ENERGEN
FDA Adverse Event
Death
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·December 14, 2012
2.15MM X 22MM SPIRAL ROUTER
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·November 27, 2013