Device recall
Z-2758-2026: P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped…
FDA device recall · Class II · Paragon 28, Inc.
Key facts
| Recall number (Z-number) | Z-2758-2026 |
|---|---|
| Recall event | 99276 |
| Product | P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm, ITem number P31-955-1800-S; provides stabilization of the hindfoot and ankle. |
| Product code | HXI |
| Recalling firm | Paragon 28, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3008650117 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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