Medtronic Perfusion Systems
Medtronic Perfusion Systems holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2024, with 116 FDA device recalls on record.
Top product codes for Medtronic Perfusion Systems
FDA recalls by Medtronic Perfusion Systems
10 most recent of 116- Z-2809-2026 — EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722
- Z-2811-2026 — EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78322
- Z-2810-2026 — EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222
- Z-2806-2026 — EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77422
- Z-2808-2026 — EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77622
- Z-2807-2026 — EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522
- Z-2739-2026 — Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
- Z-2738-2026 — Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
- Z-2576-2026 — Octopus Evolution AS Tissue Stabilizer, Model TS2500
- Z-2577-2026 — Octopus 4 Tissue Stabilizer, Model 29400
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Medtronic Perfusion Systems
- K240666 — Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface (BB811) +2 more
- K181954 — autoLog IQ Autotransfusion System
- K123351 — AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACE
- K101186 — AFFINITY VARD SUB-ASSEMBLY FOR CPS (CARMEDA COATED), PURGELINE (UNCOATED), HOLDING BAG
- K090869 — MIRCSP (MINIMALLY INVASIVE RETROGRADE CORONARY SINUS PERFUSION) MANUAL INFLATE CANNULA, MODEL 94113TD
- K080824 — BIO-CONSOLE 560
- K061254 — EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222
- K052524 — BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT
- K052372 — MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C
- K051303 — BIO-CONSOLE, MODEL 560
- K051040 — HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR
- K050109 — TRILLIUM BIOPUMP PLUS, MODEL BPX80T
- K043179 — SELECT 3D ARTERIAL CANNULA
- K041830 — MAGELLAN RATIO DISPENSER KIT
- K040173 — PEDIATRIC AORTIC ROOT CANNULA
- K033468 — AFFINITY 20U ARTERIAL FILTER WITH TRILLIUM BIOSURFACE
- K033416 — SELECT 3D ARTERIAL CANNULA WITH CARMEDA BIOACTIVE SURFACE AND SELECT CAP ARTERIAL CANNULA WITH CARMEDA BIOACTIVE SURFACE
- K033264 — MALLEABLE SINGLE STAGE VENOUS CANNULA WITH CARMEDA BIOACTIVE SURFACE, MODEL CB681XX SERIES
- K031700 — MEDTRONIC RESTING HEART SYSTEM, MODEL AAR1000 AND 711
- K031776 — MC2X MULTI-STAGE VENOUS CANNULA
- K031827 — ULTRAFLEX VENOUS CANNULA, MODEL 970XX AND CB970XX
- K031037 — EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA AND GUIDEWIRE
- K030696 — RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH NO PRESSURE LINE (15 FRENCH, MANUAL AND AUTO INFLATE)
- K021287 — TRILLIUM AFFINITY NT CARDIOTOMY VENOUS RESERVOIR, MODELS 540T, 541TT
- K020147 — MAGELLAN RATIO DISPENSER KIT/MAGELLAN SPRAY TIP/MAGELLAN CANNULA TIP
- K013084 — AFFINITY 38 MICON ARTERIAL FILTER WITH TRILLIUM BIOPASSIVE SURFACE, MODEL 351T
- K012743 — TRILLIUM TRI-OPTIC MEASUREMENT CELL, MODEL TMC 25T, TMC38 T, TMC 50T
- K012747 — TRILLIUM BIO DISPOSABLE BLOOD FLOW PROBE (MODELS DP38T & FP38P)
- K994208 — AFFINITY 20 MICRON ARTERIAL BLOOD FILTER, MODEL 353/354
Data sourced from openFDA. This site is unofficial and independent of the FDA.