Medtronic Perfusion Systems recalls
27 recalls filed under Medtronic Perfusion Systems. The most recent was published August 5, 2026.
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Class II · 3 months ago
Medtronic Perfusion Systems Eopa Elongated One-Piece Arterial Cannula Blunt 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems Eopa Elongated One-Piece Arterial Cannula Blunt 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA 3D Arterial Cannula 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic DLP One-Piece Pediatric Arterial Cannula recall: Medtronic received two complaints of loose foreign material confirmed
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
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Class II · 3 months ago
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115 recall: Medtronic received two complaints of loose foreign material confirmed
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
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Class II · 4 months ago
Medtronic Perfusion Systems Octopus Evolution Tissue Stabilizer, Model TS2000 recall: During the manufacturing process, Medtronic personnel identified an assembly
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was…
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Class II · 4 months ago
Medtronic Perfusion Systems Octopus 4 Tissue Stabilizer, Model 29400 recall: During the manufacturing process, Medtronic personnel identified an assembly
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was…
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Class II · 4 months ago
Medtronic Perfusion Systems Octopus Evolution AS Tissue Stabilizer, Model TS2500 recall: During the manufacturing process, Medtronic personnel identified an assembly
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was…
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Class II · 5 months ago
Medtronic Gundry Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic Gundry Retrograde Cannula Manual-Inflate Silicone Body 13FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 8 months ago
Medtronic Perfusion Systems Octopus Nuvo Tissue Stabilizer recall: During the manufacturing, Medtronic personnel identified an assembly issue
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached…
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Class II · 11 months ago
Medtronic Perfusion Systems MC3 VitalFlow Console, REF 58100 recall: As of August 6, 2025, Medtronic has received eleven reports of VitalFlow
As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this…
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Class II · 11 months ago
Medtronic HR-ACT , REF 402-03 recall: Medtronic personnel observed trace amounts of dry blood on the external
Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT…
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Class II · 11 months ago
Medtronic Perfusion Systems Affinity NT Oxygenator recall: Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas
Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas transfer rates that did not meet performance requirements.
About this page
Medtronic Perfusion Systems appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.