Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DLP Extension Line Adapters 20 in length Used to extend Recalled by Medtronic Perfusion Systems Due to Identification of small pinholes in a single packaging...
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 Extension Line Adapters 20 in length Used to extend cardioplegia line during cardiopulmonary bypass surgery
Quantity: 63053 (48180 US) (14873 OUS)
Why Was This Recalled?
Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.
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