Device recall
Z-1350-2020: Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for…
FDA device recall · Class II · ulrich medical USA Inc
Key facts
| Recall number (Z-number) | Z-1350-2020 |
|---|---|
| Recall event | 84638 |
| Product | Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw |
| Product code | KWP |
| Recalling firm | ulrich medical USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2025 |
| 510(k) numbers | K150650 |
| FEI number | 3005532635 |
At a glance
- 1–9 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