Device recall
Z-1788-2021: Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay…
FDA device recall · Class II · Getinge (Suzhou) Co Ltd
Key facts
| Recall number (Z-number) | Z-1788-2021 |
|---|---|
| Recall event | 87752 |
| Product | Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay system |
| Product code | FNM |
| Recalling firm | Getinge (Suzhou) Co Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 13, 2023 |
| FEI number | 3005619970 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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