| 2026-08-05 | FDA Device | FDA Recall: EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return ca | Medtronic Perfusion Systems | Class II | N/A |
| 2026-08-05 | FDA Device | FDA Recall: EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass a | Medtronic Perfusion Systems | Class II | N/A |
| 2026-08-05 | FDA Device | FDA Recall: EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass | Medtronic Perfusion Systems | Class II | N/A |
| 2026-08-05 | FDA Device | FDA Recall: EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass a | Medtronic Perfusion Systems | Class II | N/A |
| 2026-08-05 | FDA Device | FDA Recall: EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial r | Medtronic Perfusion Systems | Class II | N/A |
| 2026-08-05 | FDA Device | FDA Recall: EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass | Medtronic Perfusion Systems | Class II | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass | Medtronic Perfusion Systems | Class II | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascul | Medtronic Perfusion Systems | Class II | N/A |
| 2026-07-01 | FDA Device | FDA Recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500 | Medtronic Perfusion Systems | Class II | N/A |
| 2026-07-01 | FDA Device | FDA Recall: Octopus 4 Tissue Stabilizer, Model 29400 | Medtronic Perfusion Systems | Class II | N/A |
| 2026-07-01 | FDA Device | FDA Recall: Octopus Evolution Tissue Stabilizer, Model TS2000 | 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 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 13FR, Model 94913L; 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 94965; 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 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 94215T; Cardiopulmonar | 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 GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmona | 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 |