HomeMedical Device recalls
Medium severity

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateApril 21, 2026
ReportedMay 27, 2026
Recalling firmMedtronic Perfusion Systems
Country / regionUnited States MN

Hazard

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

Affected products

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