61 results · 41ms · 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.

QDOT MICRO

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code OAE·May 6, 2026

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·April 28, 2017

THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·February 2, 2023

PERFUSOR SPACE

FDA Adverse Event
Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·June 22, 2023

PERFUSOR SPACE

FDA Adverse Event
Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·June 22, 2023

PULSE GEN MODEL 106

FDA Adverse Event
Injury ·LIVANOVA USA, INC.·Product code LYJ·July 6, 2023

DIALOG®

FDA Adverse Event
Death ·B. BRAUN AVITUM AG·Product code KDI·August 11, 2022

PULSE GEN MODEL UNK

FDA Adverse Event
Injury ·LIVANOVA USA, INC.·Product code LYJ·July 22, 2022

DIALOG®

FDA Adverse Event
Death ·B. BRAUN AVITUM AG·Product code KDI·August 11, 2022

THERMOCOOL® SMART TOUCH® SF UNI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Death ·BIOSENSE WEBSTER INC·Product code LPB·June 26, 2023

MICROCUFF PEDIATRIC ENDOTRACHEAL TUBE, ORAL/NASAL MAGILL-8.7-6.5-20

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code BTR·December 16, 2021

DA VINCI XI

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·September 10, 2019

DAVINCI XI

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·July 11, 2024

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS - HOUSTON·Product code LYJ·September 2, 2022

LEAD MODEL 303

FDA Adverse Event
Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·September 15, 2023

NEWPORT E200 WAVE

FDA Adverse Event
Malfunction ·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·December 13, 2007

UNKNOWN ELASTOMERIC PUMP

FDA Adverse Event
Malfunction ·AVANOS - IRVINE·Product code MEB·November 19, 2018

KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 16, 2026

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code MTD·September 14, 2022

SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM

FDA Adverse Event
Death ·SHOCKWAVE MEDICAL, INC.·Product code QMG·October 5, 2023