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. The most frequent reason is sterility.

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

0Oct '24 1 0 3Jan '25 0 1 0Apr 0 0 0Jul 0 3 0Oct 3 0 0Jan '26 0 1 0Apr 9 0 5Jul 6 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

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.