Microvention, Inc.: MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, HydroSoft 3D, Sterile, Rx, REF numbers 100102HFRM-V, 100152HFRM-V, 100153HFRM-V, 100154HFRM-V, 100202HFRM-V, 100206HFRM-V, 100208HFRM-V, 100254HFRM-V, 100256HFRM-V, 100308HFRM-V, MV-00202HHTA, MV-00203HHTA, MV-00204HHTA, MV-00206HHTA, MV-00208HHTA, MV-00304HHTA, MV-00306HHTA, MV-00308HHTA, MV-00310HHTA, MV-00408HHTA, MV-00412HHTA, MV-00510HHTA, MV-00515HHTA, MV-00612HHTA, MV-00619HHTA, MV-00715HHTA, MV-00728HHTA, MV-00817HHTA, MV-00833HHTA, MV-01502HHTA, MV-01503HHTA, MV-01504HHTA, MV-02504HHTA, MV-02506HHTA, and MV-02508HHTA. Product Usage: The HES 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-1405-2020

Recalling firm

Microvention, Inc.

Product

MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, HydroSoft 3D, Sterile, Rx, REF numbers 100102HFRM-V, 100152HFRM-V, 100153HFRM-V, 100154HFRM-V, 100202HFRM-V, 100206HFRM-V, 100208HFRM-V, 100254HFRM-V, 100256HFRM-V, 100308HFRM-V, MV-00202HHTA, MV-00203HHTA, MV-00204HHTA, MV-00206HHTA, MV-00208HHTA, MV-00304HHTA, MV-00306HHTA, MV-00308HHTA, MV-00310HHTA, MV-00408HHTA, MV-00412HHTA, MV-00510HHTA, MV-00515HHTA, MV-00612HHTA, MV-00619HHTA, MV-00715HHTA, MV-00728HHTA, MV-00817HHTA, MV-00833HHTA, MV-01502HHTA, MV-01503HHTA, MV-01504HHTA, MV-02504HHTA, MV-02506HHTA, and MV-02508HHTA. Product Usage: The HES 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

847 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:  100102HFRM-V - 1903045W6 and 1903135W6;  100152HFRM-V - 1903085W6, 1903185P6, and 1903185W6;  100153HFRM-V - 1903135W6;  100154HFRM-V - 1903015W6, 1903205W6, 1903225W6, 1904225P6, and 1904225W6;  100202HFRM-V - 1903065W6, 1903085W6, and 1903135W6;  100206HFRM-V - 1903065W6 and 1903085W6;  100208HFRM-V - 1903065W6;  100254HFRM-V - 1903045W6, 1903085W6, and 1903115W6;  100256HFRM-V - 1903045W6 and 1903225W6;  100308HFRM-V - 1903115W6, 1903155W6, and 1903205W6;  MV-00202HHTA - 1903065Y6, 1903205Y6, and 1903225Y6;  MV-00203HHTA - 1903085Y6, 1903225Y6, 1904155Y6, 1905085X6, 1905085Y6, 1905105Y6, 1905175Y6, 1905205Y6, and 1905225Y6;  MV-00204HHTA - 1903085Y6, 1904155X6, 1904155Y6, 1905085Y6, 1905105Y6, 1905135Y6, 1905205Y6, and 1905225Y6;  MV-00206HHTA - 1904015Y6, 1904155X6, 1905025Y6, 1905035Y6, 1905085Y6, 1905135Y6, 1905175Y6, 1905205Y6, and 1905225Y6;  MV-00208HHTA - 1905135Y6, 1905205Y6, 1905225X6, and 1905225Y6;  MV-00304HHTA - 1903065Y6, 1903135Y6, 1903205Y6, 1904035Y6, 1905025Y6, 1905065Y6, and 1905085Y6;  MV-00306HHTA - 1903135Y6, 1903205Y6, 1903225Y6, 1904055Y6, 1904085Y6, 1904105Y6, 1905025Y6, 1905035Y6, 1905085Y6, 1905105Y6, and 1905135Y6;  MV-00308HHTA - 1905085Y6, 1905205Y6, and 1905225Y6;  MV-00310HHTA - 1905025Y6, 1905035Y6, 1905065Y6, 1905105Y6, 1905135Y6, 1905175Y6, 1905205Y6, and 1905225Y6;   MV-00408HHTA - 1903225X6, 1904035Y6, 1905025Y6, and 1905035Y6;  MV-00412HHTA - 1903115Y6, 1903135Y6, 1903205Y6, 1904035Y6, 1904055Y6, 1904085Y6, 1904105Y6, 1904225Y6, 1905025Y6, 1905035Y6, 1905065Y6, 1905085Y6, 1905105Y6, 1905135Y6, 1905175Y6, and 1905205Y6;  MV-00510HHTA - 1903225Y6, 1904035Y6, 1904055Y6, 1905085Y6, 1905105Y6, 1905175Y6, and 1905225Y6;  MV-00515HHTA - 1903225X6, 1904035Y6, 1905025Y6, 1905035Y6, 1905085Y6, 1905105Y6, 1905135Y6, 1905175X6, 1905175Y6, 1905205Y6,  and 1905225Y6;  MV-00612HHTA - 1903085Y6, 1903115Y6, 1903135Y6, 1903225X6, 1904055Y6, 1905025Y6, 1905035Y6, and 1905085Y6;   MV-00619HHTA - 1903085Y6, 1903115Y6, 1903225Y6, 1904055Y6, 1905035Y6, 1905065Y6, 1905085Y6, 1905105Y6, 1905175Y6, 1905205Y6, and 1905225Y6;   MV-00715HHTA - 1905065Y6, 1905105Y6, 1905135Y6, 1905175Y6, 1905205Y6, 1905225X6, and 1905225Y6;  MV-00728HHTA - 1905105Y6, 1905135Y6, 1905175Y6, 1905205Y6, and 1905225Y6;  MV-00817HHTA - 1905105Y6, 1905175Y6, and 1905205X6;  MV-00833HHTA - 1903085Y6, 1903205Y6, 1905035Y6, 1905085Y6, 1905135Y6, and 1905205Y6;  MV-01502HHTA - 1903085Y6, 1903205Y6, 1905025Y6, 1905105Y6, 1905175Y6, and 1905205Y6;  MV-01503HHTA - 1903085Y6, 1903115Y6, 1903135Y6, 1903205Y6, 1903225X6, 1903225Y6, 1904035Y6, and 1905035Y6;  MV-01504HHTA - 1905035Y6, 1905065Y6, and 1905085Y6;   MV-02504HHTA - 1903085Y6, 1903205Y6, 1905025Y6, 1905065Y6, 1905105Y6, 1905175Y6, 1905205Y6, and 1905225Y6;   MV-02506HHTA - 1903085Y6, 1903205Y6, 1905025Y6, 1905065Y6, 1905105Y6, 1905135Y6, 1905205Y6, and 1905225Y6; and   MV-02508HHTA - 1905085Y6, 1905105Y6, 1905135Y6, 1905155Y6, 1905205Y6, and 1905225Y6.

510(k) numbers

["K050954","K091641","K132952","K153594","K161367"]

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

Copy