Medtronic Perfusion Systems recalls

Medtronic Perfusion Systems has 116 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 5 Aug 2026. 63 are still ongoing. 24 were reported in the last 12 months.

Total recalls116since 2014

Last 12 months24reported

Class I1513% of total

Ongoing63latest 5 Aug 2026

Recalls per month, last 24 months

click a bar for that month

1Nov '24 0 3 0Feb 1 0 0May 0 0 0Aug 3 0 3Nov 0 0 0Feb 1 0 9May 0 5 6Aug 0 0

Severity split

Class I 15 13%Class II 100 86%Class III 1 1%

Why medtronic perfusion systems is recalled

Product types

By year

20262118%
2025109%
20241715%
202365%
202222%
20214034%
202011%
201933%
201843%
201754%

Ongoing medtronic perfusion systems recalls

63 active

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	Eopa Elongated One-Piece Arterial Cannula Blunt recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	Eopa Elongated One-Piece Arterial Cannula Blunt recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA 3D Arterial Cannula DIL TIP, intended for use recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA 3D Arterial Cannula, intended for use recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide

All medtronic perfusion systems recalls, newest first

116 total

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	Eopa Elongated One-Piece Arterial Cannula Blunt recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	Eopa Elongated One-Piece Arterial Cannula Blunt recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA 3D Arterial Cannula DIL TIP, intended for use recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA 3D Arterial Cannula, intended for use recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS II	EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled	Medtronic Perfusion Systems	Packaging Defects	Nationwide
22 Jul 2026Device	CLASS II	Medtronic DLP One-Piece Pediatric Arterial Cannula recalled	Medtronic Perfusion Systems	Foreign Material	Nationwide
22 Jul 2026Device	CLASS II	Medtronic Bio-Medicus Adult Cannula Kit recalled	Medtronic Perfusion Systems	Foreign Material	Nationwide
1 Jul 2026Device	CLASS II	Octopus Evolution Tissue Stabilizer recalled	Medtronic Perfusion Systems	Other	Nationwide
1 Jul 2026Device	CLASS II	Octopus 4 Tissue Stabilizer recalled by Medtronic Perfusion Systems	Medtronic Perfusion Systems	Other	Nationwide
1 Jul 2026Device	CLASS II	Octopus Evolution AS Tissue Stabilizer recalled	Medtronic Perfusion Systems	Other	Nationwide
27 May 2026Device	CLASS II	Medtronic Gundry Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic Gundry Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
27 May 2026Device	CLASS II	Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body recalled	Medtronic Perfusion Systems	Sterility	Nationwide
4 Mar 2026Device	CLASS II	Octopus Nuvo Tissue Stabilizer recalled by Medtronic Perfusion Systems	Medtronic Perfusion Systems	Other	Nationwide
26 Nov 2025Device	CLASS II	MC3 VitalFlow Console recalled by Medtronic Perfusion Systems	Medtronic Perfusion Systems	Other	Nationwide
26 Nov 2025Device	CLASS II	Medtronic Hr-act (High Range Activated Clotting Time Cartridges) recalled	Medtronic Perfusion Systems	Other	Nationwide
19 Nov 2025Device	CLASS II	Affinity NT Oxygenator, Oxygenator recalled	Medtronic Perfusion Systems	Other	AZ, CA, TN
10 Sep 2025Device	CLASS I	Dlp Left Heart Vent Catheter Malleable body recalled	Medtronic Perfusion Systems	Device Malfunction	Nationwide
10 Sep 2025Device	CLASS I	Dlp Left Heart Vent Catheter Malleable body recalled	Medtronic Perfusion Systems	Device Malfunction	Nationwide
10 Sep 2025Device	CLASS I	Dlp Left Heart Vent Catheter Malleable body recalled	Medtronic Perfusion Systems	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS I	Aortic Root Cannula: Dlp Aortic Root Cannula A. Cannula recalled	Medtronic Perfusion Systems	Other	Nationwide
29 Jan 2025Device	CLASS II	Select Series Angled Tip Arterial Cannula recalled	Medtronic Perfusion Systems	Labeling Errors	Nationwide
29 Jan 2025Device	CLASS II	EOPA Arterial Cannula recalled by Medtronic Perfusion Systems	Medtronic Perfusion Systems	Labeling Errors	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.