5 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017
AGC V2 INTERLOK TIB 10X 71MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code HRX·May 19, 2017
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERYLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 29, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 7, 2010
AGC REVISION KNEE TIBIAL AUGMENTATION
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code JWH·June 28, 2017