Device recall
Z-1000-2007: Vitatron T-Series Dual Chamber pacemaker T60 DR, model T60A1. The Vitatron C60…
FDA device recall · Class II · Medtronic Inc. Cardiac Rhythm Managment
Key facts
| Recall number (Z-number) | Z-1000-2007 |
|---|---|
| Recall event | 37587 |
| Product | Vitatron T-Series Dual Chamber pacemaker T60 DR, model T60A1. The Vitatron C60 DR is a dual chamber rate responsive pacemaker (activity sensing using an accelerometer) for permanent atrial and ventricular pacing. T-Series software VSF07/VSF08 Version 1.2. Vitatron is a division of Medtronic, Inc… |
| Product code | NVZ |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Managment |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 16, 2008 |
| FEI number | 2182208 |
At a glance
- None 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