Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2623-2014 — 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.

U.S. FDA — Device Enforcement · United States · 2014-08-15 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2623-2014
Date of alert: 2014-08-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic Cardiovascular Surgery-the Heart Valve Division
Product category: device
Product type: Devices

Reported risk: Medtronic has decided to discontinue production and distribution of this low-volume product.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2623-2014 — 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.

Related