Device recall
Z-2623-2014: Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No…
FDA device recall · Class II · Medtronic Cardiovascular Surgery-the Heart Valve Division
Key facts
| Recall number (Z-number) | Z-2623-2014 |
|---|---|
| Recall event | 69089 |
| 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. |
| Product code | DYE |
| Recalling firm | Medtronic Cardiovascular Surgery-the Heart Valve Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 6, 2014 |
| PMA numbers | P870078 |
| FEI number | 2025587 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database