Device recall
Z-1687-2021: MyWay Walker Chassis - Product Usage: is intended for use by children already…
FDA device recall · Class II · James Leckey Design Ltd
Key facts
| Recall number (Z-number) | Z-1687-2021 |
|---|---|
| Recall event | 87804 |
| Product | MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device. |
| Product code | ITJ |
| Recalling firm | James Leckey Design Ltd |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3010712784 |
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