14 results · 31ms · Sources: EU EUDAMED, US FDA

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R3 36MM ID US CRMC LINER 54

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

MAESTRO FOOT SWITCH

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

MAESTRO 4000 POD, 100W

FDA Adverse Event
Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

DRX-REVOLUTION

FDA Adverse Event
Malfunction ·CARESTREAM HEALTH, INC.·Product code IZL·March 28, 2013

FATHOM GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·March 25, 2011

ONE TOUCH ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·April 14, 2008

RESURFACING FEMORAL HEAD 50MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JDI·February 28, 2018

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·October 8, 2019

NEU_INTERSTIM_INS

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·July 12, 2012