FDA Device recall Z-2623-2014
Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012
- FDA Device
- Class II
- terminated
- Published 2014-09-17
On 2014-09-17 the FDA classified a Class II recall of Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012 by Medtronic Cardiovascular Surgery The Heart Valve Division, citing medtronic has decided to discontinue production and distribution of this low-volume product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2623-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-15 |
| Published | 2014-09-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medtronic Cardiovascular Surgery The Heart Valve Division |
| Distribution | MD, TX |
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
Medtronic has decided to discontinue production and distribution of this low-volume product.
Identifiers
| code_info | Serial Numbers: B146341, B146350 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2623-2014%22
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