FDA Device recall Z-1554-2020
NaviCare Patient Safety Software Versions 3.5.400-3.9.300
- FDA Device
- Class II
- terminated
- Published 2020-04-01
On 2020-04-01 the FDA classified a Class II recall of NaviCare Patient Safety Software Versions 3.5.400-3.9.300 by Hill Rom, citing there is a software issue which may result in failure to monitor or control patient's bed exit mechanism.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1554-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-14 |
| Published | 2020-04-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hill Rom |
| Distribution | CO, GA, IN, LA, NC, NV, OR, SC, TN, VA, WA |
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)
Reason
There is a software issue which may result in failure to monitor or control patient's bed exit mechanism.
Identifiers
| code_info | NaviCare Patient Safety Software versions 3.5.400 to 3.9.300 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2020%22
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