11 results
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52ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNK
FDA Adverse Event
Death
·*·Product code JEA·September 22, 2006
ADVIA 1800
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·October 3, 2013
ADVIA CENTUAR XP SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·February 19, 2018
SYNVISC ONE
FDA Adverse Event
Malfunction
·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·November 17, 2017
AQUACEL AG-EXUDATE MANAGEMENT HYDROFIBER
FDA Adverse Event
Injury
·CONVATEC LIMITED·Product code NAC·February 28, 2014
ALPHAXCELL
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB·Product code IKY·July 17, 2012
DURAGEN-UNKNOWN PRODUCT ID
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·August 24, 2018
BCS XP SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·September 29, 2017
XPS® BLADE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·January 30, 2023
FLOWTRON EXCEL/TRIO PUMPS
FDA Adverse Event
Other
·GETINGE (SUZHOU) CO. LTD.·Product code JOW·July 25, 2012
FLOWTRON/UNIVERSAL PUMPS
FDA Adverse Event
Malfunction
·GETINGE (SUZHOU) CO. LTD.·Product code JOW·July 17, 2012