medical MODERATE Updated 2026-07-22

Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula, Product

See all recalls from Medtronic Perfusion Systems →

Recalled Product

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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Medtronic DLP One-Piece Pediatric →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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