Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hancock Apical Left Ventricle Connector Recalled by Medtronic Cardiovascular Surgery-the Heart Valve Division Due to Medtronic has decided to discontinue production and distribution...
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
Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with Hancock Conduit Model 105 to provide an alternate method for relief of left ventricular hypertension.
Quantity: 2 units
Why Was This Recalled?
Medtronic has decided to discontinue production and distribution of this low-volume product.
Where Was This Sold?
This product was distributed to 2 states: MD, TX
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