FDA Device recall Z-1393-2020
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D, Sterile, Rx, REF numbers 100102HS3D-V…
- FDA Device
- Class II
- terminated
- Published 2020-03-04
On 2020-03-04 the FDA classified a Class II recall of MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D, Sterile, Rx, REF numbers 100102HS3D-V… by Microvention, citing the devices may be missing the implant coil.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1393-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-22 |
| Published | 2020-03-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Microvention |
| Distribution | GA |
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D, Sterile, Rx, REF numbers 100102HS3D-V, 100103HS3D-V, 100152HS3D-V, 100153HS3D-V, 100154HS3D-V, 100202HS3D-V, 100203HS3D-V, 100204HS3D-V, 100206HS3D-V, 100208HS3D-V, 100254HS3D-V, 100256HS3D-V, 100304HS3D-V, 100306HS3D-V, 100310HS3D-V, 100355HS3D-V, 100358HS3D-V, 100406HS3D-V, 100408HS3D-V, 100412HS3D-V, 100415HS3D-V, 100510HS3D-V, 100515HS3D-V; MV-00102HTDA, MV-00103HTDA, MV-00204HTDA,MV-00304HTDA, MV-00306HTDA, MV-00406HTDA, MV-00408HTDA, MV-00510HTDA, MV-01502HTDA, MV-01503HTDA, MV-01504HTDA; MV-02504HTDA, MV-02506HTDA, MV-03505HTDA, and MV-03508HTDA. Product Usage: The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature. The firm name on the label is MicroVention, Inc., Tustin, CA.
Reason
The devices may be missing the implant coil.
Identifiers
| code_info | Catalog/lot numbers: 100102HS3D-V - 1903045WT, 1903065WT, 1903205WT, 1904015WT, 1904035WT, 1904245WT, 1904255WT, 190…Catalog/lot numbers: 100102HS3D-V - 1903045WT, 1903065WT, 1903205WT, 1904015WT, 1904035WT, 1904245WT, 1904255WT, 1904265WT, 1904295WT, 1905025WT, 1905065WT, 1905085WT, 1905155WT, 1905175WT, and 1905205WT; 100103HS3D-V - 1903115TT, 1903015WT, 1903085WT, 1903135WT, 1904015WT, 1904035WT, 1904055WT, 1904105WT, 1904265WT, 1904295WT, 1905035WT, 1905105PT, 1905135WT, 1905155WT, and 1905225WT; 100152HS3D-V - 1903065NT, 1903045WT, 1903085WT, 1903205WT, 1903225WT, 1904015WT, 1904105WT, 1904175WT, 1904295WT, 1905025WT, 1905105WT, 1905135WT, 1905155WT, and 1905175WT; 100153HS3D-V - 1903015WT, 1903045WT, 1903065WT, 1903155WT, 1904015WT, 1904035WT, 1904265WT, 1904295WT, 1905135WT, and 1905205WT; 100154HS3D-V - 1903045WT, 1903085WT, 1903135WT, 1903185WT, 1903225WT, 1904015WT, 1904035WT, 1904085WT, 1904105WT, 1904155WT, 1904175WT, 1904225WT, 1905025WT, 1905135WT, 1905155PT, 1905155WT, 1905175WT, and 1905205WT; 100202HS3D-V - 1903015WT, 1903065WT, 1903185WT, 1903205WT, 1905105WT, and |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1393-2020%22
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