Medtronic Pediatric Cannula Recall: Loose Blood Material Risk

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Recalling firmMedtronic Perfusion Systems7611 Northland Dr N · Brooklyn Park, MN 55428-1088

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Medtronic is recalling pediatric arterial cannulas that may contain trace blood material. This could cause minor issues during medical procedures if the cannula becomes loose.

Why it’s dangerous

The cannula may have loose foreign material containing trace blood. This could cause minor issues during medical procedures if the cannula becomes loose.

Who’s affected

Pediatric patients undergoing surgery who use the recalled cannulas. Medical staff handling the cannulas during procedures are most at risk.

How to tell if you have this one

Check for Product Number/CFN 77010. The cannula has Lot Numbers: 0231650870 or C232227220. It was sold as a Cardiopulmonary bypass vascular cannula.

Brand
Medtronic Perfusion Systems
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Cannula Details
Verify the Product Number/CFN 77010 and Lot Numbers 0231650870 or C232227220.

✎ GovInfoNow

Questions people ask

Why is this cannula being recalled?

Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

What should I do if I have this cannula?

Check the Product Number/CFN 77010 and Lot Numbers 0231650870 or C232227220 to confirm if it's affected.

Is there a fix for this issue?

The recall record does not mention any remedy or fix.

Take action

Contact Medtronic Perfusion Systems

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

✉️ Open in email

Subject: Recall Z-2738-2026 — Medtronic Perfusion Systems Medtronic Perfusion Systems

Hello,

I own a Medtronic Perfusion Systems that is covered by recall Z-2738-2026 from Medtronic Perfusion Systems.

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-2738-2026 (May 25, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2738-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula

Lower-risk recall