13 results
·
53ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CUT/COAGULATION HANDPIECE FOR OPEN SURGERY
FDA Adverse Event
Malfunction
·PLASMA SURGICAL INC.·Product code GEI·September 6, 2013
PLASMAJET SURGICAL SYSTEM
FDA Adverse Event
Malfunction
·PLASMA SURGICAL INC.·Product code GEI·August 6, 2015
PLASMAJET CUT/COAGULATION HANDPIECE
FDA Adverse Event
Malfunction
·PLASMA SURGICAL INC.·Product code GEI·April 30, 2012
PLASMA JET
FDA Adverse Event
Malfunction
·PLASMA SURGICAL INC·Product code GEI·October 31, 2005
PLASMAJET NEUTRAL PLASMA SURGERY CONSOLE
FDA Adverse Event
Malfunction
·PLASMA SURGICAL INC.·Product code GEI·November 1, 2013
YC-1800
FDA Adverse Event
Malfunction
·NIDEK CO. LTD·Product code LXS·April 10, 2018
DA VINCI SI SURGICAL SYSTEM
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·October 31, 2013
ARTHREX ACP TM DOUBLE SYRINGE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 7, 2024
ARTHREX ACP TM DOUBLE SYRINGE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 6, 2024
DADE INNOVIN
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJS·June 23, 2017
ERBE APC HANDLE
FDA Adverse Event
Malfunction
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·June 28, 2023
ALERE DETERMINE HIV-1/2 AG/AB COMBO
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·February 24, 2020
AIA-360
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·April 18, 2018