9,639 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NJE - STENT, INTRACRANIAL NEUROVASCULAR
FDA Adverse Event
Death
·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code NJE·November 13, 2007
LVIS HDE
FDA Adverse Event
Malfunction
·MICROVENTION, INC.·Product code QCA·November 7, 2024
LVIS HDE
FDA Adverse Event
Malfunction
·MICROVENTION, INC.·Product code QCA·November 22, 2024
LVIS JR.
FDA Adverse Event
Malfunction
·MICROVENTION, INC.·Product code QCA·August 28, 2025
LVIS D
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·June 9, 2025
LVIS
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·February 23, 2026
PROWLER SELECT MICROCATHETERS
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code KRA·May 21, 2013
LVIS D
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·August 13, 2025
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·July 21, 2016
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·June 28, 2016
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·October 16, 2025
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·July 3, 2025
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·August 26, 2025
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·August 22, 2025
LVIS
FDA Adverse Event
Malfunction
·MICROVENTION, INC.·Product code QCA·August 29, 2025
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·May 21, 2025
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·March 24, 2026
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·March 30, 2026
LVIS HDE
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·March 24, 2026
Stryker brand Neuroform 3 Microdelivery Stent System, 4.5 mm X 20 mm, REF Catalog Number: E345020, Model/Product Number: M003450200, Product is manufactured by Boston Scientific Corporation, Fremont, CA and distributed by Stryker Neurovascular, Fremont, CA The Neuroform Microdelivery Stent System is intended for use with embolic coils for the treatment of wide neck, intracranial, saccular aneurysms arising from a parent vessel with a diameter of greater than equal to 2 mm and greater than equal to 4.5 mm that are not amenable to treatment with surgical clipping.
FDA Recall
Terminated
·Stryker Neurovascular·Product code NJE·June 24, 2013