Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Retrograde Cardioplegia Cannula Recalled by Surge Medical Sales, LLC (DBA Surge Cardiovascular) Due to The device was built with the rigid insertion...
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 Surge Medical Sales, LLC (DBA Surge Cardiovascular) directly.
Affected Products
Retrograde Cardioplegia Cannula, Model Number RMG-0015S The Retrograde Cardioplegia Cannula is intended for use in perfusing cardioplegia solutions retrograde through the coronary sinus by means of transatrial introduction.
Quantity: 35 units
Why Was This Recalled?
The device was built with the rigid insertion stylet instead of the flexible stylet.
Where Was This Sold?
This product was distributed to 1 state: SC
About Surge Medical Sales, LLC (DBA Surge Cardiovascular)
Surge Medical Sales, LLC (DBA Surge Cardiovascular) has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report