Device recall
Z-0050-04: Channel Neuroendoscope, Standard Resolution, 13 cm, Catalog No. 2232-003.
FDA device recall · Class III · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-0050-04 |
|---|---|
| Recall event | 27299 |
| Product | Channel Neuroendoscope, Standard Resolution, 13 cm, Catalog No. 2232-003. |
| Product code | GWG |
| Recalling firm | Medtronic Neurosurgery |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 21, 2003 |
| FEI number | 3015531529 |
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