Device recall
Z-0036-2007: Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter…
FDA device recall · Class II · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-0036-2007 |
|---|---|
| Recall event | 36072 |
| Product | Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue |
| Product code | INI |
| Recalling firm | Medline Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2009 |
| 510(k) numbers | K041054 |
| FEI number | 1417592 |
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