253 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Death
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RIB RETRACTOR
FDA Adverse Event
Death
·WECK DIV. LINVATEC INC.·Product code GAD·July 5, 1995
ON-Q PAINBUSTER POST-OP PAIN RELIEF SYSTEM
FDA Adverse Event
Death
·I-FLOW/KIMBERLY CLARK·Product code MEB·July 21, 2010
LUCAS¿ CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·February 7, 2023
AUTOPULSE RESUSCITATION SYSTEM
FDA Adverse Event
Death
·ZOLL CIRCULATION·Product code DRM·October 26, 2011
CALYPOSO
FDA Adverse Event
Death
·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FSA·August 21, 2014
FINOCHIETTO RIB SPREADER 65X65MM BLDS
FDA Adverse Event
Death
·AESCULAP AG·Product code GAD·February 20, 2019
VALIANT CAPTIVIA
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·May 13, 2014
AUTOPULSE® LIFEBAND
FDA Adverse Event
Death
·ZOLL CIRCULATION·Product code DRM·March 1, 2023
AUTOPULSE RESUSCITATION MODEL 100
FDA Adverse Event
Death
·ZOLL CIRCULATION·Product code DRM·March 1, 2023
CAPSURE EPI
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DTB·May 9, 2008
CAPSURE EPI
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DTB·May 9, 2008
KAPPA 900 DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code DXY·May 9, 2008
LUCAS 3 CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·May 12, 2021
SCREW, FIXATION, BONE
FDA Adverse Event
Death
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·November 7, 2018
PLATE, FIXATION, BONE
FDA Adverse Event
Death
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·November 7, 2018
PLATE, FIXATION, BONE
FDA Adverse Event
Death
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·November 7, 2018
HOYER PATIENT LIFTER
FDA Adverse Event
Death
·HOYER OPERATIONS·Product code FSA·July 17, 1997
ELECTRODE PEDIATRIC 4.5X6.25 DEFIB ZOLL
FDA Adverse Event
Death
·COVIDIEN·Product code DRO·April 4, 2019
LUCAS¿ CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·June 8, 2018
LIBERTY SELECT CYCLER
FDA Adverse Event
Death
·FRESENIUS·Product code FKX·June 4, 2019