Device recall
Z-0622-05: LICOX Complete Brain IMC Probe Kit, Model IM3.ST C
FDA device recall · Class III · Integra Neuro Sciences
Key facts
| Recall number (Z-number) | Z-0622-05 |
|---|---|
| Recall event | 31117 |
| Product | LICOX Complete Brain IMC Probe Kit, Model IM3.ST C |
| Product code | GMW |
| Recalling firm | Integra Neuro Sciences |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 13, 2005 |
| 510(k) numbers | K002765 |
| FEI number | 2023988 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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