MICROVENTION Recalls
38 recalls on record · September 13, 2017 to August 19, 2026 · Medical Devices
Recalls by year
17
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21
22
23
24
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26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 4, 2020Medical DevicesFDA
Microvention, Inc. recalls MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, Helical, Sterile, Rx, REF nu
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039, 4
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx. The
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-781434, 45-781639, 4
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 45-681434, 45-682050, and 45-680
Hazard: The devices may be missing the implant coil.
February 19, 2020Medical DevicesFDA
Microvention, Inc. recalls Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-4810
Hazard: The devices may be missing the implant coil.
September 13, 2017Medical DevicesFDA
Microvention, Inc. recalls MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package, sterile
Hazard: There is a potential for the hydrophilic coating on the guidewire to delaminate from the guidewire.