Device recall
Z-2488-2021: Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28…
FDA device recall · Class II · Paragon 28, Inc.
Key facts
| Recall number (Z-number) | Z-2488-2021 |
|---|---|
| Recall event | 88553 |
| Product | Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630 |
| Product code | HTW |
| Recalling firm | Paragon 28, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2021 |
| FEI number | 3008650117 |
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