8 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
X-STOP PEEK INTERSPINOUS SPACER
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NQO·February 1, 2019
CARDIOSAVE HYBRID, 3.1 EDITION
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·May 23, 2024
VARIPULSE¿ BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code QZI·May 21, 2026
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 19, 2008
TENDRIL STS
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·September 8, 2011
EASYTRAK
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·July 22, 2013
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