Device recall
Z-2822-2018: NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath…
FDA device recall · Class II · Nico Corp.
Key facts
| Recall number (Z-number) | Z-2822-2018 |
|---|---|
| Recall event | 80540 |
| Product | NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024 |
| Product code | GZT |
| Recalling firm | Nico Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2018 |
| FEI number | 3007456622 |
At a glance
- None 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