Device recall
Z-0081-2008: Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 710 Medtronic Parkway…
FDA device recall · Class III · Medtronic Inc. Cardiac Rhythm Managment
Key facts
| Recall number (Z-number) | Z-0081-2008 |
|---|---|
| Recall event | 39422 |
| Product | Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The Paceart System can act as a Practice Management software application and is intended for use by facilities that provide services such as event monitoring, trans-telephonic pacemaker… |
| Product code | DPS |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Managment |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 3, 2008 |
| 510(k) numbers | K024278 |
| FEI number | 2182208 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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