985 results · 73ms · 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.

ULTIMUM HEMOSTASIS INTRODUCER, 4F ACT, 12 CM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code DYB·August 4, 2004

AMPLATZ SUPER STIFF GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code DQX·April 2, 2008

WALLSTENT ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code FGE·April 2, 2008

INDIGO SYSTEM FLASH ASPIRATION CATHETER

FDA Adverse Event
Death ·PENUMBRA, INC.·Product code QEW·July 8, 2024

POD PACKING COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·September 20, 2016

MW5081021

FDA Adverse Event
Malfunction ·November 1, 2018

INDIGO SYSTEM LIGHTNING 12

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code QEW·November 1, 2021

ANGIOSEAL

FDA Adverse Event
Injury ·SHERWOOD MEDICAL·Product code MGB·July 26, 2000

INTERLOCK¿-35

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRD·November 8, 2011

HF SENSOR DELIVERY SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.·Product code MOM·October 15, 2024

TEMPO

FDA Adverse Event
Malfunction ·CORDIS US. CORP·Product code DQO·February 24, 2026

MYNXGRIP

FDA Adverse Event
Malfunction ·CARDINAL HEALTH SANTA CLARA·Product code MGB·February 13, 2023

EMBOSHIELD NAV6

FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code NTE·April 28, 2025

CAROTID WALLSTENT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIM·October 31, 2018

INTERLOCK?-35

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRD·October 30, 2014

.018 SV5 GUIDEWIRE

FDA Adverse Event
Injury ·CORDIS US CORP.·Product code DQX·October 16, 2024

.018 ROADRUNNER GUIDEWIRE

FDA Adverse Event
Injury ·COOK INCORPORATED·Product code DQX·October 16, 2024

PALMAZ BALLOON-EXPANDABLE STENT WITH DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS, A JOHNSON & JOPHNSON CO.·Product code MAF·December 3, 1996

PROGRAMMING SOFTWARE

FDA Adverse Event
Malfunction ·LIVANOVA USA, INC.·Product code LYJ·October 26, 2018

STARCLOSE SE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·August 13, 2009