Maquet Axius Blower Mister Recall: Risk of CO2 Flow Delay During Surgery

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Contact the company & request your remedy

Recalling firmMaquet Cardiovascular, LLC45 Barbour Pond Dr, N/A · Wayne, NJ 07470-2094

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Maquet is recalling the Axius Blower Mister device because it may not properly clear CO2 during certain heart surgeries, causing delays. This could affect surgical outcomes if the device fails to function correctly.

Why it’s dangerous

The device is designed to clear anastomotic sites during heart surgery. If it fails to maintain proper CO2 flow, it may cause delays in critical surgical steps, potentially impacting patient safety.

Who’s affected

Surgical teams using the Axius Blower Mister during off-pump coronary artery bypass procedures are most at risk. Patients undergoing these surgeries with the recalled device could experience procedural delays.

How to tell if you have this one

Check for lot numbers 96255605, 96255607, 96255608, 96255609, or 96255611 on the device. The product code is CB-1000.

Brand
Maquet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Lot Number
Look for lot numbers 96255605, 96255607, 96255608, 96255609, or 96255611 on the device.

✎ GovInfoNow

Questions people ask

What is the product code for the recalled device?

The product code is CB-1000.

What lot numbers are affected?

Lot numbers 96255605, 96255607, 96255608, 96255609, and 96255611 are affected.

Is there a remedy for this recall?

The recall record does not specify a remedy.

Take action

Contact Maquet

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

✉️ Open in email

Subject: Recall Z-0983-2019 — Maquet Maquet

Hello,

I own a Maquet that is covered by recall Z-0983-2019 from Maquet.

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-0983-2019 (January 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0983-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.

Maquet Cardiovascular, LLC recalls AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site

Lower-risk recall