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Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Recalled July 22, 2026 · FDA recall Z-2738-2026 · Medtronic Perfusion Systems
Hazard
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. · FDA Class II
Sold at
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
Description
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Product
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →