Official recall notice

FDA DeviceClass IINotable

Medtronic DLP Retrograde Cannula Recall (May 2026)

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

Recall date
2026-05-27
FDA class
Class II

Why it was recalled

Hazard

Certain lots of product have the potential for a sterile barrier breach.

One email a week when there are new recalls. Confirm by email; unsubscribe anytime.

Product description

Certain lots of product have the potential for a sterile barrier breach.

Verify with the official notice →
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