Device recall
Z-0681-2022: Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn…
FDA device recall · Class II · Acorn Stairlifts, Inc
Key facts
| Recall number (Z-number) | Z-0681-2022 |
|---|---|
| Recall event | 88610 |
| Product | Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift |
| Product code | PCD |
| Recalling firm | Acorn Stairlifts, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 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