56 results · 68ms · Sources: EU EUDAMED, US FDA

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ALTIUS SYSTEM

FDA Adverse Event
Injury ·NEUROS MEDICAL INC.·Product code SAZ·May 14, 2026

ALTIUS SYSTEM

FDA Adverse Event
Injury ·NEUROS MEDICAL INC.·Product code SAZ·May 14, 2026

ALTIUS SYSTEM

FDA Adverse Event
Injury ·NEUROS MEDICAL INC.·Product code SAZ·December 3, 2025

ALTIUS SYSTEM

FDA Adverse Event
Injury ·NEUROS MEDICAL INC.·Product code SAZ·December 3, 2025

ALTIUS SYSTEM

FDA Adverse Event
Malfunction ·NEUROS MEDICAL INC.·Product code LGW·April 2, 2025

ALTIUS SYSTEM

FDA Adverse Event
Malfunction ·NEUROS MEDICAL INC.·Product code LGW·June 20, 2025

ALTIUS SYSTEM

FDA Adverse Event
Injury ·NEUROS MEDICAL INC.·Product code SAZ·May 14, 2026

ALTIUS SYSTEM

FDA Adverse Event
Malfunction ·NEUROS MEDICAL INC.·Product code SAZ·March 31, 2025

NEURO PATTIE

FDA Adverse Event
Malfunction ·CARWILD CORP.·Product code EFQ·August 24, 2016

PERIFIX®

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL INC.·Product code OGE·October 26, 2017

HYDROFILL-10-AV

FDA Adverse Event
Malfunction ·MICROVENTION, INC.·Product code KRD·October 3, 2024

CORTRAK 2 ENTERAL ACCESS SYSTEM

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code KNT·June 7, 2023

SLIC COMPONENT: 7 FR X 6

FDA Adverse Event
Injury ·ARROW INTL., INC.·Product code DYB·July 10, 2012

O-ARM 1000 IMAGING SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·October 28, 2016

CORTRAK 2 ENTERAL ACCESS SYSTEM

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code KNT·May 8, 2023

CORTRAK 2 ENTERAL ACCESS SYSTEM

FDA Adverse Event
Death ·AVANOS MEDICAL INC.·Product code KNT·November 1, 2023

CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH ENFIT CONNECTOR

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code KNT·June 8, 2021

TECNIS SYMFONY TORIC

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code POE·May 10, 2018

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code POE·May 10, 2018

PULSE GEN MODEL 106

FDA Adverse Event
Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·June 2, 2023