Device recall
Z-1530-2016: Acorn 180 Curved Stairlift
FDA device recall · Class II · Acorn Stairlifts Inc
Key facts
| Recall number (Z-number) | Z-1530-2016 |
|---|---|
| Recall event | 73509 |
| Product | Acorn 180 Curved Stairlift |
| Product code | PCD |
| Recalling firm | Acorn Stairlifts Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2019 |
| FEI number | 3003124453 |
At a glance
- None 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