# FDA recall Z-1554-2020

> **Hill-Rom Inc.** · Class II · device recall initiated 2020-02-14.

## 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 for recall

There is a software issue which may result in failure to monitor or control patient's bed exit mechanism.

## Distribution

Colorado, Georgia, Indiana, Louisiana, North Carolina, Nevada, Oregon, South Carolina, Tennessee, Virginia, Washington.

## Key facts

- **Recall number:** Z-1554-2020
- **Recalling firm:** Hill-Rom Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-14
- **Report date:** 2020-04-01
- **Termination date:** 2021-02-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cary, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1554-2020

## Citation

> AI Analytics. FDA recall Z-1554-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1554-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*