Device recall
Z-2007-2023: NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
FDA device recall · Class II · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-2007-2023 |
|---|---|
| Recall event | 92300 |
| Product | NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed |
| Product code | FNL |
| Recalling firm | Baxter Healthcare Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1417572 |
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