Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Joseph Lamelas Atrial Lift System Recalled by Biorep Technologies Due to The support arm attached with an adhesive to...
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 Biorep Technologies directly.
Affected Products
Joseph Lamelas Atrial Lift System, Model Number MI-ALS-001. A single surgical instrument or tool for retraction of the atrial wall tissue in cardiac surgery.
Quantity: 80 boxes (480 units)
Why Was This Recalled?
The support arm attached with an adhesive to the body of the blade is detaching while attempting to engage the visor component.
Where Was This Sold?
This product was distributed to 1 state: MN
About Biorep Technologies
Biorep Technologies 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