10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019
VARIPULSE¿ BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code QZI·May 21, 2026
UNKNOWN DEPUY TIBIAL TRAY
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSH·November 19, 2008
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·September 8, 2011
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 22, 2013
LIBERTA RECHARGEABLE IPG
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code MHY·June 7, 2024
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·December 1, 2025
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·April 21, 2026
TRI-STAPLE 2.0
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·December 5, 2022
ENDO GIA ULTRA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·December 2, 2022