74 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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WHOOP WEARABLE ARMBAND
FDA Adverse Event
Injury
·WHOOP·Product code QZW·January 6, 2025
EZW
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·May 24, 2018
EZW
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·October 15, 2019
SYNERGY VERSITREL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·June 13, 2016
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 15, 2013
SYNERGY
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·September 29, 2014
INTERSTIM
FDA Adverse Event
Injury
·MPROC, JUNCO·Product code EZW·September 21, 2007
SYNERGY VERSITREL
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 22, 2014
TINED LEAD
FDA Adverse Event
Injury
·MPROC VILLALBA·Product code EZW·September 21, 2007
RESTORE PRIME
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 29, 2015
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 13, 2016
SYNERGY
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 13, 2012
SYNERGY VERSITREL
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 13, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·December 28, 2016
SYNERGY VERSITREL
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 24, 2015
INTERSTIM
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code EZW·July 25, 2008
SYNERGY VERSITREL
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 23, 2015
RESTORE PRIME
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 8, 2016
GII QA+ W #2 ORTHOCORD
FDA Adverse Event
Injury
·DEPUY MITEK·Product code JDR·December 22, 2016
GII QA+ W #2 ORTHOCORD
FDA Adverse Event
Injury
·DEPUY MITEK·Product code JDR·December 21, 2016