Device recall
Z-1235-2014: Buzzaround XL scooters' Product Usage: mobility
FDA device recall · Class II · Golden Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1235-2014 |
|---|---|
| Recall event | 67416 |
| Product | Buzzaround XL scooters' Product Usage: mobility |
| Product code | INI |
| Recalling firm | Golden Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2015 |
| 510(k) numbers | K041025 |
| FEI number | 2523955 |
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