Medtronic DLP One-Piece Pediatric Arterial Cannula recall: Foreign Material
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Why was Medtronic DLP One-Piece Pediatric Arterial Cannula recalled?
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
- Product
- Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
- Recalling firm
- Medtronic Perfusion Systems
- Distribution
- Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
- Recall date
- July 22, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)