9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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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
HIRES 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS LLC·Product code MCM·December 1, 2010
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 9, 2014
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