Microvention recalls specific endovascular embolization coils that may be missing the implant coil, risking incomplete treatment of vascular malformations.
The devices may be missing the implant coil.
Microvention is recalling certain endovascular embolization coils that may be missing the implant coil. This could lead to incomplete treatment of vascular malformations, potentially causing blood flow issues.
The recalled coils may be missing the implant coil, which is critical for properly blocking blood flow to vascular malformations. Without the correct coil, the procedure may not effectively treat the condition, leading to potential blood flow issues.
Patients undergoing endovascular procedures for vascular malformations or aneurysms who use the recalled coil systems are affected. Medical professionals using these devices for treatment are at risk if they have the recalled products.
Check for the product name 'MicroVention Terumo Microplex 10, Platinum Coil System' with specific REF numbers: 100204CC-V through 101026CC-V. The lot numbers listed in the recall record indicate the affected batches.
Verify the REF number on the label matches the listed numbers (100204CC-V to 101026CC-V) to determine if the product is affected.
The devices may be missing the implant coil, which is critical for properly blocking blood flow to vascular malformations.
Check the REF number on the label to see if it matches the listed numbers (100204CC-V to 101026CC-V). If it does, contact Microvention for further instructions.
The recall indicates a potential risk of incomplete treatment, but the hazard does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1400-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1400-2020 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.
