Device recall
Z-0522-06: The product is a mobile 3-wheeled electric scooter, model HMV 250. The product…
FDA device recall · Class II · Tung Keng Enterprise Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0522-06 |
|---|---|
| Recall event | 34405 |
| Product | The product is a mobile 3-wheeled electric scooter, model HMV 250. The product contains either a red or blue base. The red base is identified with SKU #915363224. The blue base is identified with SKU #915363225. The product is distributed by the Invacare Corporation. |
| Product code | INI |
| Recalling firm | Tung Keng Enterprise Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| 510(k) numbers | K033240 |
| FEI number | 3002667030 |
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