Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to Incorrect labeling for seven manufactured lots of certain...
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
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Quantity: 930 units
Why Was This Recalled?
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
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