6 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HWE·December 30, 2025
CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HWE·December 30, 2025
ACCU-CHEK MULTICLIX LANCETS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code FMK·November 20, 2008
INNOVA 2000
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·August 17, 2011
COMPREHENSIVE PRIMARY STEM 12MM MINI
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·July 22, 2013
CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HWE·January 20, 2026