Microvention, Inc.: 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.

Recall number

Z-1400-2020

Recalling firm

Microvention, Inc.

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.

Status

Terminated

Initiated

2019-11-22

Posted

not on file

Terminated

2022-01-26

Reason

The devices may be missing the implant coil.

Root cause

Process design

Action

The recalling firm issued letters beginning 11/22/2019 dated 11/26/2019 via email using different flags according to the region the foreign consignee was located, i.e. 'URGENT: FIELD SAFETY CORRECTION ACTION" (for EMEA), "URGENT: MEDICAL DEVICE RECALL" (for Japan), or "FIELD SAFETY ADVISORY NOTICE" (for Rest of World).

Quantity

409 units

Distribution

All distribution was OUS. The countries receiving affected product are: Albania, Austria, Belarus, Belgium, Brazil, Bulgaria, China, Cyprus, Czech Republic, Denmark, Egypt, Finalnd, France, Georgia, Germany, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Latvia, Lebanon, Malta, Morocco, Netherlands, Norway, Poland, Portugal, Republic of Serbia, Romania, Russian Federation, Slovak Republic, Slovenia, South Africa, Spain, Sweden, Switzerland, Syria, Turkey, Ukraine, United Arab Emirates, and United Kingdom.

Lot, serial or model codes

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.

510(k) numbers

["K050954","K131948","K132952","K153594"]

PMA numbers

not on file

Product code

HCG

Firm FEI

3003523199

Firm city

Aliso Viejo

Firm state

CA

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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