Device recall
Z-0174-2008: Electric Mobility Corporation (EMC)- Scooters and Turnabout Powerchairs with…
FDA device recall · Class II · Electric Mobility Corp
Key facts
| Recall number (Z-number) | Z-0174-2008 |
|---|---|
| Recall event | 37879 |
| Product | Electric Mobility Corporation (EMC)- Scooters and Turnabout Powerchairs with either an Electric Seat Lift Actuator or a Seat Post to attach the seat to the vehicle; Model Number(s) 300F, 600C, 600T, and 600F. Electronic Mobility Corporation, 599 Mantua Blvd, One Mobility Plaza, Sewell, NJ 08080 |
| Product code | INI |
| Recalling firm | Electric Mobility Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 8, 2014 |
| 510(k) numbers | K924515 |
| FEI number | 2246975 |
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