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MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft...

FDA Device Recall #Z-1407-2020 — Class II — November 22, 2019

Recall Summary

Recall Number Z-1407-2020
Classification Class II — Moderate risk
Date Initiated November 22, 2019
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Microvention, Inc.
Location Aliso Viejo, CA
Product Type Devices
Quantity 5,777 units

Product Description

MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft Helical, Sterile, Rx, REF numbers 100101HS-V, 100102HS-V, 100103HS-V, 100104HS-V, 100151HS-V, 100152HS-V, 100153HS-V, 100154HS-V, 100201HS-V, 100202HS-V, 100203HS-V, 100204HS-V, 100206HS-V, 100254HS-V, 100256HS-V, 100304HS-V, 100306HS-V, 100308HS-V, 100406HS-V, 100408HS-V, and 100508HS-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 for Recall

The devices may be missing the implant coil.

Distribution Pattern

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 Information

Catalog/lot numbers: 100101HS-V - 1903045UH, 1903065UH, 1903115UH, 1903135UH, 1903155UH, 1903185UH, 1903205UH, 1903225UH, 1903225ZH, 1904085UH, 1904105UH, 1904175UH, 1904245UH, 1905025UH, 1905085UH, 1905105ZH, 1905135UH, 1905175UH, 1905205UH, 1905205ZH, 1905225UH, 1905225ZH, 1903135WH, 1904175WH, 1905085WH, 1905105PH, and 1905135WH; 100102HS-V - 1903115UH, 1903135UH, 1903155UH, 1903185UH, 1903205UH, 1903225UH, 1903225ZH, 1905085UH, 1905105UH, 1905105ZH, 1905135UH, 1905155UH, 1905155ZH, 1905175UH, 1905205UH, 1905205ZH, 1905225UH, 1905225ZH, 1904035WH, and 1905155WH; 100103HS-V - 1903115UH, 1903135UH, 1903155UH, 1903185UH, 1903205UH, 1903225UH, 1904105UH, 1904155UH, 1904175UH, 1904225UH, 1904245UH, 1905025UH, 1905025ZH, 1905035UH, 1905035ZH, 1905065UH, 1905085UH, 1905105UH, 1905105ZH, 1905135UH, 1905155UH, 1905155ZH, 1905175UH, 1905205UH, and 1905085WH; 100104HS-V - 1903115UH, 1903135UH, 1903225UH, 1904085UH, 1904105UH, 1904155UH, 1905085UH, 1905105UH, 1905105ZH, 1905135UH, 1905155UH, 1905155ZH, 1905175UH, 1905205UH, 1904175WH, 1904225WH, and 1905155WH; 100151HS-V - 1905025UH, 1903135TH, 1903085WH, 1903205WH, 1904015WH, 1904265WH, 1904295WH, 1905085WH, 1905155WH, and 1905225PH; 100152HS-V - 1903155UH, 1903185UH, 1903205UH, 1904085UH, 1904105UH, 1904155UH, 1904225UH, 1904245UH, 1905025UH, 1905025ZH, 1905035UH, 1905035ZH, 1905065UH. 1905085UH, 1905105UH, 1905135UH, 1905155UH, 1905155ZH, 1905175UH, 1905205ZH, 1903065NH, 1904175TH, 1904225NH, 1905065NH, 1903015WH, 1903065WH, 1903185WH, 1904015WH, 1904035WH, 1904055WH, 1904085WH, 1904155WH, 1904225WH, 1904245WH, 1904265WH, 1904295WH, 1905025WH, 1905035PH, 1905035WH, 1905065WH, 1905085WH, 1905155WH, and 1905225WH; 100153HS-V - 1903225UH, 1905105UH, 1905135UH, 1905135ZH, 1905155UH, 1905175UH, 1905205UH, 1905225UH, 1905225ZH, 1903015NH, 1903065WH, 1903085WH, 1903205WH, 1904015WH, 1904035WH, 1904055WH, 1904155WH, 1904175WH, 1904225PH, 1904225WH, 1904245WH, 1904265WH, 1905025WH, 1905035PH, 1905065WH, 1905085WH, 1905155WH, 1905205PH, 1905225PH, and 1905225WH. 100154HS-V - 1903155UH, 1903185UH, 1903205UH, 1903225UH, 1905085UH, 1905105UH, 1905105ZH, 1905135UH, 1905155UH, 1905155ZH, 1905175UH, 1905205UH, 1905225UH, 1903115TH, 1903015WH, 1903045WH, 1903065WH, 1904035WH, 1904055WH, 1904225WH, 1904245WH, 1904265WH, 1904295WH, 1905035PH, 1905035WH, 1905065WH, 1905085WH, 1905155PH, 1905155WH, 1905175WH, and 1905205WH; 100201HS-V - 1903135UH 100202HS-V - 1904085UH, 1904105UH, 1904175UH, 1904245UH, 1904225NH, 1905065NH, 1905205NH, 1903085WH, 1904015WH, 1904055WH, 1904175WH, 1904245WH, 1904265WH, 1904295WH, 1905085WH, 1905225PH, and 1905225WH; 100203HS-V - 1903155UH, 1903185UH, 1903225UH, 1904225NH, 1905135NH, 1903015WH, 1903065WH, 1904035WH, 1904225WH, 1904245WH, 1904265WH, 1904295WH, 1905035WH, 1905155WH, and 1905225WH; 100204HS-V - 1904085UH, 1904105UH, 1904225UH, 1904245UH, 1905065UH, 1905085UH, 1905105UH, 1905135UH, 1905135ZH, 1905155UH, 1905175UH, 1905205UH, 1903045WH, 1903065WH, 1904015WH, 1904035WH, 1904155WH, 1904175WH, 1904225PH, 1904245WH, 1904265WH, 1904295WH, 1905025WH, 1905035WH, 1905085WH, 1905155WH, and 1905225WH; 100206HS-V - 1904085UH, 1904105UH, 1904155UH, 1904175UH, 1904265UH, 1905065UH, 1905085UH, 1905105UH, 1905105ZH, 1905135UH, 1905155UH, 1905175UH, 1905205UH 1905205ZH, 1905225UH, 1903065WH, 1903085WH, 1903185WH, 1904055WH, 1904175WH, 1904225WH, 1904245WH, 1904265WH, 1904295WH, 1905025WH, 1905035PH, 1905035WH, 1905065WH, 1905155WH, 1905175WH, and 1905225WH; 100254HS-V - 1903205WH, 1904015WH, 1904225WH, 1904265WH, 1904295WH, 1905025WH, 1905085WH, and 1905225PH; 100256HS-V - 1903065WH, 1903185WH, 1904015WH, and 1905155WH; 100304HS-V - 1903085NH, 1903135TH, 1904035TH, 1903065WH, 1905035PH, and 1905065WH; 100306HS-V - 1903115UH, 1903135UH, 1903155UH, 1903185UH, 1904085UH, 1903065WH, 1904035WH, 1904055WH, 1904155WH, 1904175WH, 1904225WH, 1904245WH, 1905035PH, 1905065WH, 1905205PH, and 1905225PH; 100308HS-V - 1903185UH, 1903225UH, 1905135UH, 1905175UH, 1905205UH, 1903085NH, 1903015WH, 1903065WH, 1903185WH, 1904015WH, 1904035WH, 1904055WH, 1904175WH, 1904225WH, 1904245WH, 1904265WH, 1904295WH, 1905025WH, 1905035PH, 1905035WH, and 1905065WH; 100406HS-V - 1903085WH, 1903185WH, 1904035WH, 1904225WH, and 1905205WH; 100408HS-V - 1905085UH, 1905105UH, 1905135UH, 1905155UH, 1903115TH, 1903015WH, 1903065WH, 1904265WH, 1904295WH, 1905085WH, 1905135WH, 1905155WH, and 1905205PH; 100508HS-V - 1903225TH, 1905205NH, 1903015WH, 1903085WH, 1903135WH, 1903185WH, 1904265WH, 1905105WH, and 1905205WH.

Other Recalls from Microvention, Inc.

Recall # Classification Product Date
Z-1224-2020 Class II Terumo AZUR Peripheral Coil System, Detachable ... Nov 24, 2019
Z-1225-2020 Class II Terumo AZUR CX Peripheral Coil System, Detachab... Nov 24, 2019
Z-1223-2020 Class II Terumo AZUR Peripheral Coil System, Detachable ... Nov 24, 2019
Z-1220-2020 Class II Terumo AZUR Peripheral Coil System, Detachable ... Nov 24, 2019
Z-1222-2020 Class II Terumo AZUR CX Peripheral Coil System, Detachab... Nov 24, 2019

Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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