Class II U.S. Food and Drug Administration

Medtronic DLP One-Piece Pediatric Arterial Cannula recall: Medtronic received two complaints of loose foreign material confirmed

Recall published 3 months ago

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

The hazard: Foreign material — foreign objects

The company found foreign objects in the product, or a customer did. Either way the recall covers every pack from the runs listed, because contamination of this kind is rarely confined to one unit.

What the notice says: Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

Why it matters: Pieces of foreign objects may be inside the product. The risk here is physical rather than microbial: cuts to the mouth or throat, a broken tooth, or an injury further down if a fragment is swallowed.

Symptoms and when to call a doctor

If someone has swallowed a fragment and has mouth or throat pain, trouble swallowing, chest or stomach pain, vomiting, or blood in saliva or stool, they should be seen the same day. A fragment swallowed without symptoms usually passes on its own, but tell the clinician exactly what the product was: whether it shows up on imaging depends entirely on the material, so describe the product and the notice to them.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
Z-2738-2026
Published
July 22, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Medtronic Perfusion Systems
Product type
Medical devices
Distribution
Nationwide
Made in
United States
Lot / code info
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
UPC codes
7630009466801, 20763000946689

Products covered by this recall

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

Check your product

The notice names 5 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 7630009466801
  • 20763000946689

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 0231650870
  • C232227220

Model or item number

On the rating label, the box or the instruction sheet.

  • CFN 77010

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Foreign material

Medtronic Perfusion Systems — The company found foreign objects in the product, or a customer did. Either way the recall covers every pack from the runs listed, because contamination of this kind is rarely confined to one unit.

  1. Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.
  2. Return it to the store or bin it sealed, and claim the refund using the lot code from the label.
  3. Check the freezer and the pantry for other packs carrying the same codes before you consider the matter closed.
  4. If someone has already bitten into something hard, have them stop, spit out what is in their mouth and rinse rather than swallow.

Refunds, and what else you can claim

The purchase price is the floor, not the ceiling. Where a recall caused you a real cost, say so.

  • Claim the refund at the store first; it is the fastest route and needs the least paperwork.
  • If you bought several packs over time, list them. Firms routinely settle for more than a single unit when a customer asks.
  • Medical costs, lost earnings or a spoiled event are not handled at the service desk. Write to the company contact on this page instead, with dates and documents.
  • Keep copies of everything you send. If a recall caused harm, that file is what any later claim rests on.

Company contact: Medtronic Perfusion Systems — 7611 Northland Dr N, Brooklyn Park, MN, 55428-1088

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Medtronic Perfusion Systems medical devices recalled?

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

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 7630009466801, 20763000946689; lot code 0231650870, C232227220; model number CFN 77010. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.

Can I get my money back?

Claim the refund at the store first; it is the fastest route and needs the least paperwork.

Where was the recalled product sold?

It was distributed nationwide.

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