6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·November 24, 2010
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 3, 2014
ACCU-CHEK TENDER LINK
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·December 21, 2012
ARCOS MODULAR REVISION SYSTEM CONE PROXIMAL BODY TYPE 1 TAPER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·February 22, 2017
ACTIVE ARTICULATION HIP SYSTEM DUAL MOBILITY BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·February 22, 2017
G7 OSSEOTI ACETABULAR SHELL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·February 22, 2017