Microvention recalls specific AZUR Peripheral Coil System models due to potential missing implant coils. Affected units include REF numbers 45-481015 and others. Contact for remedy details.
The devices may be missing the implant coil.
Microvention is recalling certain AZUR Peripheral Coil System devices that may be missing the implant coil. This could lead to improper treatment during medical procedures, potentially causing complications.
The devices may have missing implant coils, which could result in incomplete treatment during procedures. This might cause complications like bleeding or incomplete blockage of blood vessels.
Patients undergoing neurointervention procedures who use the recalled devices are affected. Medical professionals using the devices for embolization treatments are at risk.
Check for REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-480610, 45-480615, 45-480620, 45-480815, 45-480820, or model codes like MV-AZ80520HL. The devices are sterile and distributed by Terumo Medical Corporation.
Look for REF numbers or model codes on the device label to confirm if it's affected.
The devices may be missing the implant coil, which could lead to incomplete treatment during medical procedures.
Check for REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-480610, 45-480615, 45-480620, 45-480815, 45-480820, or model codes like MV-AZ80520HL.
The recall does not specify a remedy, so contact Microvention or Terumo Medical Corporation 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-1220-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1220-2020 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.
