Microvention Terumo AZUR Peripheral Coil System Recall: Missing Implant Coil Hazard

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Contact the company & request your remedy

Recalling firmMicrovention, Inc.35 Enterprise · Aliso Viejo, CA 92656-2601

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Microvention is recalling certain Terumo AZUR Peripheral Coil System models because they might be missing the implant coil. This could lead to improper medical treatment if the coil isn't properly placed during surgery.

Why it’s dangerous

The devices may be missing the implant coil, which is critical for proper surgical placement. If the coil is missing, the procedure might not work correctly, leading to ineffective treatment.

Who’s affected

Patients who received the recalled Terumo AZUR Peripheral Coil System models during surgery are affected. Medical professionals using these specific models for procedures are at risk.

How to tell if you have this one

Check the product label for the REF numbers 45-651026 or 45-652050. Look for lot numbers like 19030655Y, 19041556W, 19051058A for the first model and 19030654Y, 19041556X for the second model.

Brand
Microvention
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for REF numbers 45-651026 or 45-652050 on the device label.

✎ GovInfoNow

Questions people ask

What is the specific model number of the recalled device?

The recalled devices have REF numbers 45-651026 and 45-652050.

How can I tell if my device is affected?

Check the label for REF numbers 45-651026 or 45-652050 and corresponding lot numbers.

What should I do if I have the recalled device?

The recall record does not specify a remedy, so contact Microvention for further instructions.

Take action

Contact Microvention

We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1224-2020 — Microvention Microvention

Hello,

I own a Microvention that is covered by recall Z-1224-2020 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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Where this comes from

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.

Official source: FDA Recall #Z-1224-2020 (November 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1224-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Microvention, Inc. recalls Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx. The

Lower-risk recall