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