Medical DeviceMar 4, 2020
MicroVention Terumo Microplex 18, Platinum Embolization Coil, Cosmos 18, Sterile, Rx, REF recall — FDA Z-1399-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Recall history in this database
Classification mix: Class II: 31, Class III: 3.
Medical DeviceMar 4, 2020
MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil recall — FDA Z-1405-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceMar 4, 2020
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil recall — FDA Z-1396-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceMar 4, 2020
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil recall — FDA Z-1393-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers recall — FDA Z-1225-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers recall — FDA Z-1221-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil recall — FDA Z-1220-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil recall — FDA Z-1223-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers recall — FDA Z-1222-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers recall — FDA Z-1224-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Microvention, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.