4 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTMATE II LVAS
FDA Adverse Event
Malfunction
·THORATEC CORP.·Product code DSQ·February 12, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2012
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.·Product code JDI·August 26, 2010
DVR CROSSLOCK 1.7 MM SQUARE DRIVER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWR·December 13, 2017