Device recall
Z-1773-2026: XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number…
FDA device recall · Class II · XTANT Medical Holdings, Inc
Key facts
| Recall number (Z-number) | Z-1773-2026 |
|---|---|
| Recall event | 98541 |
| Product | XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL. |
| Product code | MNI |
| Recalling firm | XTANT Medical Holdings, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K152132 |
| FEI number | 3005031160 |
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