22 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 22, 2025
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 22, 2025
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 3, 2025
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 27, 2025
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 12, 2025
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 13, 2026
EXPRESS VASCULAR SD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·April 18, 2011
EXPRESS SD RENAL/BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 11, 2025
LAMBOTTE OSTEOTOME STR 1/4IN W LGTH 9IN
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code HWM·July 13, 2017
MEDEGEN ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FPA·March 19, 2013
DARCO HEADED 2.55 MM K-WIRE
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·August 12, 2014
VITALITY
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 15, 2011
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
CARPENTIER-MCCARTHY-ADAMS IMR ETLOGIX MITRAL ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·May 2, 2013
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·October 28, 2014
SINGLE USE BILIARY DRAINAGE STENT V
FDA Adverse Event
Injury
·AOMORI OLYMPUS CO., LTD.·Product code FGE·October 4, 2024
EVIS LUCERA DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDT·October 4, 2024
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 15, 2015
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 15, 2015