4 results
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15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 30, 2026
MINMED QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 3, 2024
ABC PROBE
FDA Adverse Event
Malfunction
·CONMED ELECTROSURGERY·Product code GEI·January 25, 2008
ASSURE WEARABLE CARDIOVERTER DEFIBRILLATOR
FDA Adverse Event
Malfunction
·KESTRA MEDICAL TECHNOLOGIES, INC.·Product code MVK·November 19, 2025