Device recall
Z-0304-2017: 4205 Journey Rolling Walker Product Usage: used to assist people in walking
FDA device recall · Class II · Nova Ortho-Med Inc
Key facts
| Recall number (Z-number) | Z-0304-2017 |
|---|---|
| Recall event | 75408 |
| Product | 4205 Journey Rolling Walker Product Usage: used to assist people in walking |
| Product code | ITJ |
| Recalling firm | Nova Ortho-Med Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 6, 2017 |
| FEI number | 3002329391 |
At a glance
- None 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