Device recall
Z-2405-2021: Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy…
FDA device recall · Class II · Clarus Medical, Llc
Key facts
| Recall number (Z-number) | Z-2405-2021 |
|---|---|
| Recall event | 88399 |
| Product | Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002 |
| Product code | GEX |
| Recalling firm | Clarus Medical, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2022 |
| 510(k) numbers | K040424, K922881 |
| FEI number | 1000116142 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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