1,838 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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NXSTAGE SYSTEM ONE
FDA Adverse Event
Death
·NXSTAGE MEDICAL, INC.·Product code KDI·November 26, 2014
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·April 8, 2011
NXSTAGE DIALYSATE CONCENTRATE SAK
FDA Adverse Event
Malfunction
·NXSTAGE·Product code KDI·November 1, 2017
SAKS VINE KIT
FDA Adverse Event
Malfunction
·ROSS PRODUCTS DIV. ABBOTT LABORATORIES·Product code KNT·July 8, 1996
FRESENIUS NXSTAGE CONTROL UNIT NX2000-1
FDA Adverse Event
Malfunction
·NXSTAGE MEDICAL, INC.·Product code FKR·May 11, 2022
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·August 30, 2013
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·November 16, 2010
SAK/C CERVICAL INTERBODY
FDA Adverse Event
Other
·ZIMMER SPINE·Product code HTO·January 7, 2008
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Injury
·COOK INC·Product code MIH·December 1, 2010
PUREFLOW SL
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KPO·July 30, 2008
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·July 7, 2014
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·October 19, 2012
DIALYSATE SACK WITH CONCENTRATE (SAK-302)
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KPO·March 7, 2023
CAVITRON PLUS TAP-ON, 115V G136
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·September 9, 2022
NXSTAGE SYSTEM ONE
FDA Adverse Event
Death
·NXSTAGE MEDICAL, INC.·Product code KDI·November 20, 2015
CAVITRON JET PLUS W/TAPON -115V G137
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·June 26, 2023
CAVITRON 300 SERIES G310SCLR
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·June 6, 2023
CAVITRON SELECT SPS G124 GENERATOR(DNA)
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·May 4, 2023
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·October 23, 2009
CAVITRON JET PLUS G137
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·April 4, 2023