Medtronic Perfusion Systems

Frequent Recalls

10

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-03-04 to 2026-05-27

Date	Source	Product	Brand	Severity	Units
2026-05-27	FDA Device	FDA Recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmona	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmo	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonar	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary	Medtronic Perfusion Systems	Class II	N/A
2026-05-27	FDA Device	FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonar	Medtronic Perfusion Systems	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1	Medtronic Perfusion Systems	Class II	N/A

Medtronic Perfusion Systems Recalls | WatchRecall