18 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·UNKNOWN·Product code CAW·January 22, 2013
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 12, 2021
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 20, 2021
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 6, 2018
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 22, 2021
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 15, 2019
RADIFOCUS GUIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·March 26, 2024
RADIFOCUS GUIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·February 8, 2024
RADIFOCUS GUIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·March 12, 2024
RADIFOCUS GUIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·March 12, 2024
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 28, 2019
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 22, 2019
RADIFOCUS GUIDEWIRE OR GLIDEWIRE OR GLIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 28, 2018
RADIFOCUS GUIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·December 28, 2023
RADIFOCUS GLIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 25, 2026
RADIFOCUS GLIDEWIRE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 7, 2026
RADIFOCUS GUIDEWIRE M
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 8, 2019