Device recall
Z-0559-03: Spine-Tech Ancillary Discectomy Instrument (Box Curette), Catalog Number…
FDA device recall · Class II · Sulzer Spine-Tech
Key facts
| Recall number (Z-number) | Z-0559-03 |
|---|---|
| Recall event | 25421 |
| Product | Spine-Tech Ancillary Discectomy Instrument (Box Curette), Catalog Number 07.00254.001, in Spine-Tech Ancillary Discectomy Instrument Set, Catalog Number 07.00316.001. |
| Product code | LXH |
| Recalling firm | Sulzer Spine-Tech |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2003 |
| FEI number | 1000115775 |
At a glance
- None 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