33 results · 32ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Death ·PHILIPS NORTH AMERICA LLC·Product code MHX·December 28, 2021

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

ADVIA 1800

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CEM·April 26, 2013

VITALITY 2

FDA Adverse Event
Death ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·May 6, 2011

HARMONIC ACE 36 CM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 17, 2008

JAWS STAPLE SYSTEM

FDA Adverse Event
Injury ·PARAGON 28, INC.·Product code JDR·October 20, 2017

VERIFLEX¿

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

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

VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

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

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

UNKNOWN AQUAMANTYS GENERATOR

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

UNKNOWN AQUAMANTYS GENERATOR

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

UNKNOWN OXFORD FEMORAL COMPONENT

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 15, 2018

UNKNOWN OXFORD TIBIAL COMPONENT

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 15, 2018

UNKNOWN OXFORD BEARING

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 15, 2018