Device recall
Z-0503-2015: Crocodile (size 3) are two-armed, wheeled walking aids, used by children with…
FDA device recall · Class II · Snug Seat Inc
Key facts
| Recall number (Z-number) | Z-0503-2015 |
|---|---|
| Recall event | 69665 |
| Product | Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The Crocodile is a walking aid for children with disabilities, who need supplementary assistance with their daily walking. The Crocodile is available in three sizes and can be used for children… |
| Product code | IOR |
| Recalling firm | Snug Seat Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2017 |
| 510(k) numbers | K934560 |
| FEI number | 1053060 |
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