medical Class II Updated 2020-03-04

Microvention, Inc. recalls MicroVention Terumo Microplex 10, Platinum Coil System, Endo

Recalled 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.

Hazard / Issue

The devices may be missing the implant coil.

Issued by

FDA

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/Code Info: 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 1905205WT; 100203HS3D-V - 1904015WT, 1904035WT, 1904265WT, 1904295WT, 1905065WT, 1905085WT, 1905155WT, and 1905225PT; 100204HS3D-V - 1903015WT, 1903045WT, 1903065WT, 1903085WT, 1904035WT, 1904055WT, 1904085WT, 1904245WT, 1904255WT, 1904295WT, 1905035WT, 1905065WT, and 1905085WT; 100206HS3D-V - 1904175WT, 1904225WT, 1904245WT, 1905105WT, 1905155PT, and 1905155WT; 100208HS3D-V - 1903085WT, 1903155WT, 1904035WT, 1905155PT, and 1905155WT; 100254HS3D-V - 1903015WT, 1903065WT, 1904015WT, 1904035WT, 1904055WT, 1904155WT, 1904225WT, 1904245WT, 1905035PT, 1905065WT; 100256HS3D-V - 1903015WT, 1903045WT, 1903065WT, 1903085WT, 1904015WC, 1904015WT, 1904035WT, 1904175WT, 1904245WT, 1904255WT, 1904265WT, 1904295WT, 1905035WH, 1905035WT, 1905155PT, and 1905225WT; 100304HS3D-V - 1903065WT, 1903115WT, 1903155WT, 1903205WT, 1904015WT, 1904055WT, 1904255WT, 1905105WT, 1905175WT, and 1905205WT; 100306HS3D-V - 1903085NT, 1903015WT, 1903085WT, 1903115WT, 1903135WT, 1903155WT, 1904015WT, 1904035WT, 1904055WT, 1904085WT, 1904225PT, 1904225WT, 1904245WT, 1904255WT, 1904265WT, 1905135WT, 1905175WT, and 1905205WT; 100310HS3D-V - 1903085WT and 1904035WT; 100355HS3D-V - 1903045WT, 1903085WT, 1904015WT, 1904225PT, 1904225WT, and 1905175WT; 100358HS3D-V - 1903065WT, 1904255WT, 1904265WT, 1904295WT, 1905035WT, 1905065WT, 1905085WT, 1905155WT, and 1905175WT; 100406HS3D-V - 1903015WT, 1903115WT, 1903205WT, 1904015WT, and 1905205WT; 100408HS3D-V - 1905205NT,1903085WT, 1903205WT, 1904015WT, 1904035WT, 1904055WT, 1904175WT, 1904225PT, 1904225WT, 1904255WT, 1904265WT, 1904295WT, 1905025WT, 1905105WT, 1905155WT, and 1905175WT; 100412HS3D-V - 1903135WT, 1904035WT, 1904175WT, and 1905105WT; 100415HS3D-V - 1903135WT, 1904035WT, 1905105WT, and 1905155WT; 100510HS3D-V - 1903065WT, 1904015WT, 1904035WT, 1904245WT, 1905105WT, and 1905155WT; 100515HS3D-V - 1903085NT, 1903015WT, 1903045WT, 1903085WT, 1903185WT, 1903205WT, 1904015WT, 1904035WT, 1904175WT, 1904265WT, 1904295WT, 1905025WT, 1905035WT, 1905085WT, 1905175WT; MV-00102HTDA - 1903015YT, 1903045YT, 1903155XT, 1904105YT, and 1904155XT; MV-00103HTDA - 1903045YT, 1903185YT, 1905065YT, and 1905085YT; MV-00204HTDA - 1904085YT and 1905065YT; MV-00304HTDA - 1905085YT; MV-00306HTDA - 1903015YT, 1903155XT, and 1903155YT; MV-00406HTDA - 1903015YT, 1904055YT, 1905065YT, and 1905085YT; MV-00408HTDA - 1903155YT, 1904015XT, 1904085YT, 1905035XT, 1905065YT, and 1905085YT; MV-00510HTDA - 1904085YT and 1905085YT; MV-01502HTDA - 1903015YT, 1904085YT, 1904105YT, 1905085YT, and 1905105YT; MV-01503HTDA - 1904055YT, 1904085YT, 1905085YT, 1905105XT, and 1905135YT; MV-01504HTDA - 1904085YT, 1904105YT, 1905085YT, 1905105XT, 1905105YT, 1905135YT, and 1905155YT; MV-02504HTDA - 1903155YT, 1904055YT, and 1905085YT; MV-02506HTDA - 1903155YT, 1905085YT, and 1905105YT; and MV-03505HTDA - 1903015YT, 1903155YT, 1904085YT, 1905085YT, and 1905105YT; and MV-03508HTDA - 1904055YT, 1904085YT, 1905085YT, and 1905105XT.
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →

Related medical Recalls

Boston Scientific Corporation recalls Boston Scientific Guider Softip XF, 40 XF, 8F, Guide Cathete

2022-08-31 · The impacted products were distributed with an MPXF tip curve shape instead of the 40XF tip curve shape for the Guider/40XF/8FR/90CM guide catheter.

Mckesson Medical-Surgical Inc. Corporate Office recalls MEDLINE INDUSTRIES Medline Plug, Catheter Medline Plastic, w

2022-08-31 · Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

GE Healthcare, LLC recalls (1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (

2022-08-31 · Inaccurate Distance and Area measurements with use of Global Stack viewport.

Mckesson Medical-Surgical Inc. Corporate Office recalls B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY,

2022-08-31 · Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.