Device recall
Z-1009-03: Pulsar Max II Multiprogrammable Pacemaker, Model 1180
FDA device recall · Class II · Guidant Corp-Cpi Division
Key facts
| Recall number (Z-number) | Z-1009-03 |
|---|---|
| Recall event | 26561 |
| Product | Pulsar Max II Multiprogrammable Pacemaker, Model 1180 |
| Product code | DXY |
| Recalling firm | Guidant Corp-Cpi Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2004 |
| FEI number | 2124215 |
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