4,975 results · 38ms · 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.

ROCHE ACCUCHEK INFORM METERS

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS·Product code NBW·September 28, 2009

FULLFIRE SELECT DIFFUSE TIP PROBE

FDA Adverse Event
Malfunction ·MONTERIS MEDICAL CORPORATION·Product code GEX·August 5, 2016

BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 21, 2025

BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·April 3, 2025

BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 24, 2025

PYXIS MEDSTATION ES SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION 303·Product code BRY·January 8, 2025

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 2, 2025

BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 18, 2025

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·August 6, 2025

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 31, 2025

BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·July 14, 2025

BD PYXIS MEDSTATION ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 31, 2024

ADVANTA V12 COVERED STENT

FDA Adverse Event
Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·March 18, 2021

AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·LOMBARD MEDICAL LTD.·Product code MIH·December 17, 2014

AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·LOMBARD MEDICAL LTD·Product code MIH·December 17, 2014

AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·LOMBARD MEDICAL LTD·Product code MIH·December 17, 2014

ASG-300R

FDA Adverse Event
Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·August 1, 2018

MULTISTIX 8 SG

FDA Adverse Event
Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JIO·May 10, 2013

MULTISTIX 9 SG

FDA Adverse Event
Malfunction ·BAYER CORP. DIAGNOSTICS DIV.·Product code CFR·June 5, 1997

AORFIX AAA FLEXIBLE STENT GRAFT

FDA Adverse Event
Injury ·LOMBARD MEDICAL LTD.·Product code MIH·January 22, 2016