fda_recall · device_recall · high

Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94…

Event date
2026-05-27 00:00:00Z
Observed
2026-07-09 22:52:27Z
Source ID
Z-2220-2026
Payload hash
37edca23f047d712b31deb53

Summary

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

Informational only. Not legal, financial, or medical advice.