Device recall
Z-2323-2008: Medtronic Patient programmer, model 37742. The Patient programmer is a hand…
FDA device recall · Class III · Medtronic Neuromodulation
Key facts
| Recall number (Z-number) | Z-2323-2008 |
|---|---|
| Recall event | 48752 |
| Product | Medtronic Patient programmer, model 37742. The Patient programmer is a hand held, battery operated, microcontroller based device for use by patients to control and monitor external and implantable devices. The minimum amount of control involves the ability to tun therapy ON or OFF; maximal control… |
| Product code | LGW |
| Recalling firm | Medtronic Neuromodulation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 21, 2008 |
| PMA numbers | P840001, P840001S086 |
| FEI number | 2182207 |
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