Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic DPL Single Stage Venous Cannula with Metal Tip Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due to Potential for uncharacteristically rough metal edges to occur...
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 Inc. Cardiac Rhythm Disease Management directly.
Affected Products
Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318; 69320; 69322; 69324; 69328; 69331.
Quantity: 13,691 (6711 USA; 6980 OUS)
Why Was This Recalled?
Potential for uncharacteristically rough metal edges to occur along the inner diameter of the metal tip side ports of the cannula.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Inc. Cardiac Rhythm Disease Management has 23 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report