Device recall
Z-2471-2008: Medtronic Adjustable Valve, 6248VAL, Sterilized using irradiation. Medtronic…
FDA device recall · Class II · Medtronic Inc. Cardiac Rhythm Managment
Key facts
| Recall number (Z-number) | Z-2471-2008 |
|---|---|
| Recall event | 49433 |
| Product | Medtronic Adjustable Valve, 6248VAL, Sterilized using irradiation. Medtronic, Inc. Minneapolis, MN 55432, USA. The Medtronic model 6248VAL adjustable valve is an accessory designed for use with Medtronic delivery systems to reduce blood loss during percutaneous catheter procedures. It consists of an… |
| Product code | DTL |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Managment |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2011 |
| 510(k) numbers | K052459 |
| FEI number | 2182208 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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