7,282 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SYNCHROMED II
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·November 21, 2016
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·May 21, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 9, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 9, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 17, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 17, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·May 8, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·March 9, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·February 24, 2026
TL,WIRE, BAYONET, 1.8MM X 400MM
FDA Adverse Event
Malfunction
·ORTHOFIX SRL·Product code KTT·March 30, 2016
TL+ METAL DISTRACTION / COMPRESSION NUT
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code LXT·August 8, 2019
TL+ METAL DISTRACTION / COMPRESSION NUT
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code LXT·August 8, 2019
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·September 15, 2006
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·September 15, 2006
ATL
FDA Adverse Event
Other
·PHILLIPS·Product code ITX·July 15, 2004
ATL
FDA Adverse Event
Injury
·ATL·Product code GDF·December 14, 2001
BTL EMSELLA
FDA Adverse Event
Injury
·BTL INDUSTRIES JSC·Product code KPI·March 29, 2019
EMSELLA BTL
FDA Adverse Event
Injury
·BTL INDUSTRIES JSC·Product code KPI·December 26, 2023
BARD TL CVC CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·November 14, 2022
BARD TL PICC
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·November 11, 2022