Device recall
Z-2821-2020: Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is…
FDA device recall · Class II · ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Key facts
| Recall number (Z-number) | Z-2821-2020 |
|---|---|
| Recall event | 86065 |
| Product | Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment. |
| Product code | FNL |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2021 |
| FEI number | 3007420694 |
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