17 results · 33ms · Sources: EU EUDAMED, US FDA

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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

AFX

FDA Adverse Event
Malfunction ·ENDOLOGIX, INC.·Product code MIH·January 22, 2016

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

NEXGEN LPS-FLEX GSF FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·April 3, 2013

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 9, 2011

ANT-CER 2 LVL PLATE ASSY, 44MM

FDA Adverse Event
Injury ·Product code KWQ·May 7, 2008

3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM

FDA Adverse Event
Malfunction ·BIOMET 3I·Product code DZE·March 12, 2018

3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM

FDA Adverse Event
Injury ·BIOMET 3I·Product code DZE·January 27, 2020

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

3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 13MM

FDA Adverse Event
Injury ·BIOMET 3I·Product code DZE·March 31, 2020

3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM

FDA Adverse Event
Injury ·BIOMET 3I·Product code DZE·July 31, 2019