Device recall
Z-0557-2013: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport…
FDA device recall · Class II · ThyssenKrupp Access Corp
Key facts
| Recall number (Z-number) | Z-0557-2013 |
|---|---|
| Recall event | 62826 |
| Product | ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors. |
| Product code | ILK |
| Recalling firm | ThyssenKrupp Access Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2014 |
| 510(k) numbers | K121560 |
| FEI number | 1925312 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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