Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic DLP Vessel Cannula Recalled by Medtronic Perfusion Systems Due to Medtronic is writing to inform you of incorrect...
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 Vessel Cannula, Model Number REF 30000
Quantity: 4343 units
Why Was This Recalled?
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
Where Was This Sold?
US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
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