70 results · 18ms · Sources: EU EUDAMED, US FDA

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APPLE WATCH SERRIES 10

FDA Adverse Event
Malfunction ·APPLE INC.·Product code QZW·September 29, 2025

EZW

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·December 14, 2009

UNKNOWN STIMULATOR

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·February 24, 2017

TINED LEAD

FDA Adverse Event
Malfunction ·MPROC, VILLALBA·Product code EZW·September 21, 2007

INTERSTIM

FDA Adverse Event
Malfunction ·MPROC, JUNCOS·Product code EZW·September 21, 2007

PRIMEADVANCED

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 2, 2014

HAMILTON MEDICAL AG

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·March 1, 2024

EXTERNAL NEUROSTIMULATOR

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 14, 2018

PRIMEADVANCED

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 29, 2015

SYNERGY

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 14, 2015

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK·Product code JDR·October 31, 2017

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK·Product code JDR·November 29, 2017

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 27, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·August 2, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·August 11, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·August 11, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 26, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 26, 2023

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 9, 2018

GII QA+ W #2 ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 9, 2018