47 results
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52ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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HEARTWARE® VENTRICULAR ASSIST SYSTEM - APEX CORING TOOL
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·July 12, 2019
X-CORE
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code MQP·November 3, 2025
FOOTPRINT ULTRA PK SUTURE ANCHOR 5.5
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code MBI·May 31, 2019
HEARTWARE VENTRICULAR ASSIST SYSTEM - APEX CORING TOOL
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·April 10, 2018
MEDTRONIC NAVIGATION
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·October 18, 2024
LOANER CORE UNIVERSAL DRIVER
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·April 15, 2014
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Malfunction
·HEARTWARE, INC·Product code DSQ·July 29, 2016
DAVINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·February 6, 2020
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Malfunction
·HEARTWARE, INC·Product code DSQ·September 16, 2015
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·May 31, 2016
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 5, 2010
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 21, 2016
O-ARM IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OXO·October 18, 2024
DEVICE FORTIFY 20MM CORE, HEIGHT 41-64MM
FDA Adverse Event
Malfunction
·GLOBUS MEDICAL, INC.·Product code NKB·March 13, 2015
M6-C
FDA Adverse Event
Malfunction
·SPINAL KINETICS LLC·Product code MJO·May 2, 2019
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·October 20, 2017
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·March 1, 2018
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·January 26, 2018
NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code MQP·July 25, 2024
NUVASIVE X-CORE EXPANDABLE VBR SYSTEM, NUVASIVE X-CORE MINI CERVICAL EXPANDABLE
FDA Adverse Event
Malfunction
·NUVASIVE, INCORPORATED·Product code MQP·November 1, 2023