Microvention recalls endovascular embolization coils that may be missing implant coils. Check product labels for REF numbers 100102HFRM-V to MV-02508HHTA. Contact Microvention for details.
The devices may be missing the implant coil.
Microvention is recalling endovascular embolization coils that may be missing the implant coil. This could lead to improper treatment of vascular malformations or aneurysms. Affected products have specific reference numbers listed in the recall notice.
The devices may be missing the implant coil, which is critical for properly blocking blood flow to aneurysms or vascular malformations. Without the coil, the procedure may not work as intended, potentially requiring additional treatments.
Medical professionals who use Microvention's HydroSoft 10 and HydroCoil Embolic Systems for endovascular procedures are most at risk. Patients receiving these treatments may also be affected if they have the recalled products.
Check the product label for reference numbers starting with 100102HFRM-V through MV-02508HHTA. The product includes specific lot numbers and catalog codes listed in the recall notice.
Look for reference numbers on the label that match the list provided in the recall notice.
The devices may be missing the implant coil, which is critical for properly blocking blood flow to aneurysms or vascular malformations.
Check the product label for reference numbers starting with 100102HFRM-V through MV-02508HHTA, along with specific lot numbers listed in the recall notice.
The recall notice does not specify a remedy, so contact Microvention directly for further instructions.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1405-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1405-2020 from Microvention. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
