22 results · 26ms · Sources: EU EUDAMED, US FDA

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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