Device recall
Z-0115-2014: Breeze C Scooter is a motorized electric scooter for elderly people. Brand name…
FDA device recall · Class II · S.A.E. AFIKIM
Key facts
| Recall number (Z-number) | Z-0115-2014 |
|---|---|
| Recall event | 66410 |
| Product | Breeze C Scooter is a motorized electric scooter for elderly people. Brand name Breeze, model C. It is intended to provide increased mobility for elderly and/or disabled person and it is also an aid to independent living. Products can be identified by their color; the recalled products are either… |
| Product code | INI |
| Recalling firm | S.A.E. AFIKIM |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2014 |
| 510(k) numbers | K102304 |
| FEI number | 1000646143 |
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