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

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

Medtronic Perfusion SystemsHealth & Personal CareMedical DevicesMATNR A7630009466801/UDI/DI 20763000946689Lot Numbers: 0231650870C232227220

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 25, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 25, 2026
Hazard Level
HIGH
Brand
Medtronic Perfusion Systems
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medtronic Perfusion Systems
Model numbers
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 25, 2026

  2. Reported by FDA DEVICE

    July 22, 2026

  3. RecallRadar source check

    July 28, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medtronic Perfusion Systems or your healthcare provider for instructions. Notification method: Letter

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Full Description

Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula. Reason: Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.. Classification: Class II. Distribution: Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
MATNR A7630009466801/UDI/DI 20763000946689
Lot Numbers: 0231650870
C232227220
Affected States
ALL
Report Date
July 22, 2026
Recall Status
ACTIVE

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