Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to EOPA Arterial Cannula Devices in this lot were...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Perfusion Systems directly.
Affected Products
Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.
Quantity: 221 (111 US, 110 OUS)
Why Was This Recalled?
EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Perfusion Systems
Medtronic Perfusion Systems has 96 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report