Device recall
Z-1554-2020: NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient…
FDA device recall · Class II · Hill-Rom Inc.
Key facts
| Recall number (Z-number) | Z-1554-2020 |
|---|---|
| Recall event | 85010 |
| Product | NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is compatible with the following beds: 1. VersaCare Revision A-J with upgrade kit Revision K with UCB 1.18 2. Centrella (all versions) 3. Progressa (firmware version 1.15.0.0) |
| Product code | KMI |
| Recalling firm | Hill-Rom Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 11, 2021 |
| FEI number | 2027454 |
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