Device recall
Z-2972-2026: Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A…
FDA device recall · Class III · Paragon 28, Inc.
Key facts
| Recall number (Z-number) | Z-2972-2026 |
|---|---|
| Recall event | 99504 |
| Product | Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant |
| Product code | PLF |
| Recalling firm | Paragon 28, Inc. |
| Recall class | Class III |
| 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