10 results
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95ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LCC - PEEK 5 DEGREES MEDIUM SPACER - 10MM X 20MM X 8MM
FDA Adverse Event
Malfunction
·ALPHATEC SPINE INC·Product code MQP·February 12, 2015
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 30, 2015
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 30, 2015
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 30, 2015
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 29, 2015
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 29, 2015
ASCENSION PHS
FDA Adverse Event
Other
·ASCENSION ORTHOPEDICS, INC.·Product code KYI·October 30, 2007
NAVILYST MEDICAL/VAXCEL
FDA Adverse Event
Injury
·NAVILYST MEDICAL·Product code LJT·October 20, 2011
SMART PORT CT
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC·Product code LJT·December 8, 2025
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 8, 2019