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Medical Device

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter

Recall date: 2026-05-27 · Source: FDA_DEVICE
Brand / Firm
Medtronic Perfusion Systems
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
Reason for recall
Certain lots of product have the potential for a sterile barrier breach.
Units affected
481 units
Description
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
View official recall notice →