Device recall
Z-2401-2016: Invacare Foot Section for Semi & Full Electric Beds, Junction Boxes, Product…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-2401-2016 |
|---|---|
| Recall event | 73577 |
| Product | Invacare Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours. |
| Product code | FNL |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2017 |
| FEI number | 1525712 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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