Device recall
Z-1824-2023: 'n'-Hole Post which is a component of the Revolution External Fixation System…
FDA device recall · Class II · New Standard Device Inc
Key facts
| Recall number (Z-number) | Z-1824-2023 |
|---|---|
| Recall event | 92390 |
| Product | 'n'-Hole Post which is a component of the Revolution External Fixation System Catalog Numbers: 100801, 100802, 100803, 100804, 100805 |
| Product code | KTT |
| Recalling firm | New Standard Device Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K181630 |
| FEI number | 3013365802 |
At a glance
- 1–9 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