Medtronic Perfusion Systems: 51 recalls on record

Recalls filed with 1 agency: FDA (51).

First recall on record: December 17, 2014. Most recent: August 5, 2026.

Risk classification: Class I: 2 · Class II: 48 · Class III: 1

Most recent recalls

DateAgencyProduct
August 5, 2026FDAEOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an…Z-2810-2026
August 5, 2026FDAEOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arteria…Z-2811-2026
August 5, 2026FDAEOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmona…Z-2807-2026
August 5, 2026FDAEOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmo…Z-2808-2026
August 5, 2026FDAEOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmona…Z-2806-2026
August 5, 2026FDAEOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmo…Z-2809-2026
July 22, 2026FDAMedtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary by…Z-2739-2026
July 22, 2026FDAMedtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmo…Z-2738-2026
July 1, 2026FDAOctopus 4 Tissue Stabilizer, Model 29400Z-2577-2026
July 1, 2026FDAOctopus Evolution Tissue Stabilizer, Model TS2000Z-2575-2026
July 1, 2026FDAOctopus Evolution AS Tissue Stabilizer, Model TS2500Z-2576-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Car…Z-2216-2026
May 27, 2026FDAMedtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; …Z-2214-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Card…Z-2221-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Card…Z-2217-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Card…Z-2219-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Card…Z-2222-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Card…Z-2218-2026
May 27, 2026FDAMedtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Ca…Z-2215-2026
May 27, 2026FDAMedtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Car…Z-2220-2026
November 19, 2025FDAAffinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous…Z-0487-2026
September 10, 2025FDADLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 1…Z-2481-2025
March 19, 2025FDAAortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, mod…Z-1306-2025
November 13, 2024FDAMedtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary …Z-0289-2025
September 18, 2024FDAMedtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312Z-3128-2024

Questions about this company

How many recalls does Medtronic Perfusion Systems have?
Recalert has 51 U.S. recalls on record for Medtronic Perfusion Systems, published between December 17, 2014 and August 5, 2026.
What was the most recent Medtronic Perfusion Systems recall?
FDA recall Z-2810-2026, published August 5, 2026: EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222
Which agencies have handled Medtronic Perfusion Systems recalls?
Medtronic Perfusion Systems appears as the recalling firm in recalls from: FDA (51).

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