7,347 results · 31ms · 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.

CADD-LEGACY PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·July 23, 2018

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·March 10, 2023

GZ-130PA

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code DRT·June 12, 2023

EXCITEOSA

FDA Adverse Event
Malfunction ·SIGNIFIER MEDICAL TECHNOLOGIES LTD·Product code QNO·June 3, 2021

EXCITEOSA

FDA Adverse Event
Malfunction ·SIGNIFIER MEDICAL TECHNOLOGIES LTD·Product code QNO·June 28, 2021

EXCITEOSA

FDA Adverse Event
Malfunction ·UNKNOWN·Product code QNO·June 28, 2023

SIGNIFIER MEDICAL EXCITE OSA

FDA Adverse Event
Malfunction ·SIGNIFIER MEDICAL TECHNOLOGIES LIMITED·Product code QNO·March 11, 2022

PIPELINE VANTAGE WITH SHIELD TECHNOLOGY

FDA Adverse Event
Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 6, 2024

ON-Q PAIN RELIEF SYSTEM WITH SELECT-A-FLOW, 400 ML, 2-14 ML/HR

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code MEB·March 18, 2025

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 6, 2021

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 26, 2023

EVEREST BICOAG

FDA Adverse Event
Malfunction ·GYRUS ACMI·Product code GEI·April 18, 2017

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 30, 2023

OPTIMA COIL SYSTEM

FDA Adverse Event
Malfunction ·BALT USA·Product code HCG·August 26, 2020

HEART START XL

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 15, 2011

INO VENT

FDA Adverse Event
Malfunction ·INO THERAPEUTICS·Product code MRN·November 22, 2004

INO VENT

FDA Adverse Event
Malfunction ·INO THERAPEUTICS·Product code MRN·December 7, 2004

INO THERAPEUTICS

FDA Adverse Event
Malfunction ·INO THERAPEUTICS·Product code CBK·May 7, 2001

INO THERAPEUTICS

FDA Adverse Event
Malfunction ·INO THERAPEUTICS·Product code CBK·May 7, 2001

INO THERAPEUTICS

FDA Adverse Event
Malfunction ·INO THERAPEUTICS·Product code MRN·May 7, 2001