38 results · 47ms · 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
Injury ·NEUROS MEDICAL INC.·Product code SAZ·May 14, 2026

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

CORTRAK 2 ENTERAL ACCESS SYSTEM

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

DA VINCI SURGICAL SYSTEM

FDA Adverse Event
Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·March 9, 2016

PULSE GEN MODEL 1000

FDA Adverse Event
Injury ·CYBERONICS - HOUSTON·Product code LYJ·November 21, 2022

TITAN BIPOL BAY FINE TIP .5MM STR FORCEP

FDA Adverse Event
Injury ·CAREFUSION, INC·Product code GEI·December 10, 2020

LAMITRODE TRIPPLE LEAD 16C, 60 CM LENGTH

FDA Adverse Event
Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 17, 2008

EON 16-CHANNEL IPG

FDA Adverse Event
Injury ·ADVANCED NEUROMODULATION SYSTEMS INC.·Product code LGW·September 17, 2008

150 ML ANGIOGRAPHIC SYRINGE FOR MEDRAD MARK V INJ.

FDA Adverse Event
Injury ·COEUR LABORATORIES, INC.·Product code DXT·August 25, 1997

TECNIS IOL

FDA Adverse Event
Injury ·AMO PUERTO RICO MFG. INC.·Product code MFK·March 16, 2023

GENERATOR MODEL 1000-D

FDA Adverse Event
Injury ·HOUSTON·Product code LYJ·June 13, 2025

QDOT MICRO

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code OAE·February 25, 2026