Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula Recalled by Medtronic Perfusion Systems Due to Potential for unsealed sterile packing.
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 I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Quantity: 7935 units
Why Was This Recalled?
Potential for unsealed sterile packing.
Where Was This Sold?
Worldwide distribution.
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