7 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·June 14, 2021
AFFINITY IV BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code HDD·December 4, 2012
VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MZP·November 30, 2010
FIBEROPTIX ULTRA 8 IAB: 8FR 30CC
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·October 2, 2022
GALAXY G3 MINI 1MM X 2CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·September 8, 2020
GALAXY G3 MINI 1MM X 3CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·September 8, 2020
GALAXY G3 MINI 1.5MM X 3CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·August 25, 2021