Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled by Medtronic Cardiovascular Surgery-the Heart Valve Division Due to Medtronic, Inc. initiated a recall of Medtronic Mosaic...
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 Cardiovascular Surgery-the Heart Valve Division directly.
Affected Products
Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
Quantity: 8276 units
Why Was This Recalled?
Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305 used with the Mosaic Porcine Aortic Bioprosthesis, Model Number 305, because of higher-than-expected transvalvular gradients occurring post implant.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Cardiovascular Surgery-the Heart Valve Division
Medtronic Cardiovascular Surgery-the Heart Valve Division has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report