39 results · 33ms · Sources: EU EUDAMED, US FDA

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VERIFLEX¿

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013

VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·June 17, 2010

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 22, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 22, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 3, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 27, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 12, 2025

UNKNOWN MICROMATRIX

FDA Adverse Event
Injury ·INTEGRA - ACELL(COLUMBIA)·Product code KGN·February 12, 2025

HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·February 23, 2024

IDRT, UNKNOWN

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·February 12, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 13, 2026

ALARIS PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION CORP·Product code FPA·March 19, 2013

ACUITY

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code OJX·April 15, 2011

RADIAL JAW 3 LARGE CAPACITY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCL·June 12, 2008

EXPRESS VASCULAR SD

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·April 18, 2011

UNKNOWN AQUAMANTYS DEVICE

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·March 10, 2017

UNKNOWN MAE GENERATOR

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·February 8, 2019

UNKNOWN AQM DEVICE

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·February 8, 2019

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·January 13, 2014

UNKNOWN AQUAMANTYS DEVICE

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·March 10, 2017