11 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ALTIUS SYSTEM
FDA Adverse Event
Malfunction
·NEUROS MEDICAL INC.·Product code LGW·April 2, 2025
ALTIUS SYSTEM
FDA Adverse Event
Malfunction
·NEUROS MEDICAL INC.·Product code LGW·June 20, 2025
STARCLOSE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·November 12, 2008
ACCESS
FDA Adverse Event
Malfunction
·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·August 31, 2011
ALARIS SE PUMP
FDA Adverse Event
Injury
·CAREFUSION CORPORATION·Product code FRN·July 10, 2013
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·January 19, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 9, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 6, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·March 26, 2018
TRI-STAPLE 2.0
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·August 7, 2023
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 14, 2018