Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip Recalled by Medtronic Perfusion Systems Due to During manufacturing, DLP Single Stage Venous Cannulae -...
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 DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Quantity: 290 units
Why Was This Recalled?
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
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