Device recall
Z-1238-2022: PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
FDA device recall · Class II · Oakworks Inc
Key facts
| Recall number (Z-number) | Z-1238-2022 |
|---|---|
| Recall event | 90172 |
| Product | PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19 |
| Product code | FNL |
| Recalling firm | Oakworks Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2024 |
| FEI number | 1000121370 |
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