7 results
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16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
1923569-2018-00016
FDA Adverse Event
Malfunction
·July 26, 2018
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 23, 2022
SNOWDEN-PENCER
FDA Adverse Event
Malfunction
·STERIS CORPORATION·Product code GEI·July 10, 2025
S-L SIDE LOADING RET HAND-AL.
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code GZT·August 21, 2019
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013
FREER SEPTUM ELEVATORS DOUBLE ENDED 7.5"
FDA Adverse Event
Malfunction
·SITE-1923569-V. MUELLER/SURGICAL GROUP·Product code GEG·April 2, 1997
FOGARTY HUDRAGRIP CLAMP
FDA Adverse Event
Malfunction
·STE - 1923569 - V. MUELLER/SURGICAL GROUP·Product code DXC·February 20, 1997