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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-2811-2026 - EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78322 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2810-2026 - EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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