FDA Device recall Z-1400-2020

MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Complex 10, Sterile, Rx, REF numbers 100204CC-V, 10…

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, Complex 10, Sterile, Rx, REF numbers 100204CC-V, 10… by Microvention, citing the devices may be missing the implant coil.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1400-2020
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, Complex 10, Sterile, Rx, REF numbers 100204CC-V, 100307CC-V, 100410CC-V, 100512CC-V, 100615CC-V, 100718CC-V, 100820CC-V, 100924CC-V, and 101026CC-V. 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: 100204CC-V -1905085LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904245WX, 190426… Catalog/lot numbers: 100204CC-V -1905085LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904245WX, 1904265WX, and 1904295WX; 100307CC-V - 1903205WX, 1904015WX, 1904225WX, 1904245WX, 1904265WX, and 1905225WX; 100410CC-V - 1904015WX, 1904175PX, 1904175WX, 1904225WX, 1904245WX, 1904265WX, 1905025WX, 1905065WX, 1905155WX, 1905205WX, and 1904035QX; 100512CC-V - 1903115LX, 1905205LX, 1903045WX, 1903205PX, 1903205WX, 1904225WX, 1905175WX, 1905205WX, 1904225RX, and 1905135RX; 100615CC-V - 1903085WX, 1903205WX, 1904225WX, 1904265WX, 1905105WX, 1905175WX, and 1905225PX; 100718CC-V - 1903115LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904265WX, 1905105WX, and 1905175WX; 100820CC-V - 1905175LX, 1904175WX, 1905025WX, 1905065PX, and 1905135RX; 100924CC-V - 1905175LX, 1904175WX, 1905065PX, 1905155WX, and 1904225RX; and 101026CC-V - 1905105LX, 1905175LX, 1905205LX, 1904175WX, 1904225WX, and 1905065PX.

code_info

Catalog/lot numbers: 100204CC-V -1905085LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904245WX, 190426…

Catalog/lot numbers: 100204CC-V -1905085LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904245WX, 1904265WX, and 1904295WX; 100307CC-V - 1903205WX, 1904015WX, 1904225WX, 1904245WX, 1904265WX, and 1905225WX; 100410CC-V - 1904015WX, 1904175PX, 1904175WX, 1904225WX, 1904245WX, 1904265WX, 1905025WX, 1905065WX, 1905155WX, 1905205WX, and 1904035QX; 100512CC-V - 1903115LX, 1905205LX, 1903045WX, 1903205PX, 1903205WX, 1904225WX, 1905175WX, 1905205WX, 1904225RX, and 1905135RX; 100615CC-V - 1903085WX, 1903205WX, 1904225WX, 1904265WX, 1905105WX, 1905175WX, and 1905225PX; 100718CC-V - 1903115LX, 1905175LX, 1905205LX, 1903185WX, 1903205WX, 1904225WX, 1904265WX, 1905105WX, and 1905175WX; 100820CC-V - 1905175LX, 1904175WX, 1905025WX, 1905065PX, and 1905135RX; 100924CC-V - 1905175LX, 1904175WX, 1905065PX, 1905155WX, and 1904225RX; and 101026CC-V - 1905105LX, 1905175LX, 1905205LX, 1904175WX, 1904225WX, and 1905065PX.

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-1400-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.