10,000 results
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57ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAXCORE
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 25, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·October 11, 2017
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·June 23, 2021
ARMADA
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LIT·August 15, 2024
SINGLE USE ASPIRATION NEEDLE NA-U200H
FDA Adverse Event
Injury
·AOMORI OLYMPUS CO., LTD.·Product code FCG·July 31, 2024
EVIS LUCERA DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDT·July 31, 2024
XIENCE PROA EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code NIQ·August 14, 2024
ARMADA
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LIT·September 13, 2024
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·August 2, 2024
SYNCHRO 2 GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC WEST VALLEY CITY·Product code DQX·October 9, 2009
ULTAMET MTL INS NEUT 36MM 54OD
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code KWA·March 19, 2013
TRANSEND EX 014/205 SOFT TIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC COSTA RICA·Product code DQX·March 27, 2013
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·November 10, 2025
MINI TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·November 20, 2018
ARCOS 3.5MM HEX DRIVE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LZO·August 12, 2020
MINI TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code LOX·November 19, 2020
AMPLATZ SUPERSTIFF GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - COSTA RICA·Product code EZB·February 8, 2011
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 21, 2022
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Death
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 21, 2022
FEMORAL TRIAL SLAPHAMMER
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·November 7, 2018