Device recall
Z-2050-2026: Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc…
FDA device recall · Class II · Centinel Spine, Inc.
Key facts
| Recall number (Z-number) | Z-2050-2026 |
|---|---|
| Recall event | 98721 |
| Product | Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement. |
| Product code | MJO |
| Recalling firm | Centinel Spine, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P070001, P070001S019, P070001S025 |
| FEI number | 3007494564 |
At a glance
- None 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