Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to Potential for a wire protrusion through the left...
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
DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only
Quantity: 51,494 units
Why Was This Recalled?
Potential for a wire protrusion through the left heart vent catheter tip
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