7,282 results · 42ms · Sources: EU EUDAMED, US FDA

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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