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

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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 AZUR CX Peripheral Coil Systems for possible missing implant coils. This could cause medical complications if the coil is needed for proper treatment.

Why it’s dangerous

The devices may be missing the implant coil, which is critical for the medical procedure. Without the coil, the treatment could be ineffective or cause complications.

Who’s affected

Patients who received the recalled AZUR CX Peripheral Coil System (detachable 35) with specific reference numbers or MV-AX codes. Those with the implant coil missing may face treatment complications.

How to tell if you have this one

Check the reference numbers on the product label: 45-751019, 45-751324, 45-751632, 45-752039, or MV-AX codes like MV-AX50407CD. The product is sterile and distributed by Terumo Medical Corporation.

Brand
Microvention
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for reference numbers on the label: 45-751019, 45-751324, 45-751632, 45-752039, or MV-AX codes like MV-AX50407CD.

✎ GovInfoNow

Questions people ask

What is the hazard with these devices?

The devices may be missing the implant coil, which is critical for the medical procedure.

How can I tell if I have a recalled product?

Check the reference numbers on the product label: 45-751019, 45-751324, 45-751632, 45-752039, or MV-AX codes like MV-AX50407CD.

What should I do if I have a recalled product?

The recall 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-1225-2020 — Microvention Microvention

Hello,

I own a Microvention that is covered by recall Z-1225-2020 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-1225-2020 (November 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1225-2020 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 CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039,

Lower-risk recall