Hancock Apical Left Ventricle Connector — Class II medical device recall Z-2623-2014
Terminated recall by Medtronic Cardiovascular Surgery-the Heart Valve Division, reported 2014-09-17, distributed in MD, TX. Medtronic has decided to discontinue production and distribution of this low-volume product.
| Recall number | Z-2623-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Cardiovascular Surgery-the Heart Valve Division, Santa Ana, CA, United States |
| Recall initiated | 2014-08-15 |
| Classified | 2014-09-11 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2014-11-06 |
| Distributed | MD, TX |
| Quantity | 2 units |
| Serial numbers | B146341, B146350 |
| Model numbers | 0174ACP012, 105, H174AXX |
Product
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.
Reason for recall
Medtronic has decided to discontinue production and distribution of this low-volume product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2623-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.