---
title: "NaviCare Nurse Call System provides a comprehensive communication and informa... — FDA record Z-1093-2022 | Is It on Recall"
description: "Firm discovered a firmware memory leak with a supplier-manufactured component."
url: https://isitonrecall.com/recall/fda-device-z-1093-2022-navicare-nurse-call-system-provides-a-comprehensive-communication-and-information-system-that-places/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# NaviCare Nurse Call System provides a comprehensive communication and information system that places patient calls, s... — FDA record Z-1093-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 13, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: NaviCare Nurse Call System provides a comprehensive communication and information system that places patient calls, staff calls, and emergency calls.
- **Reason**: Firm discovered a firmware memory leak with a supplier-manufactured component.
- **Classification**: Class II
- **Recalling firm**: Baxter Healthcare Corporation
- **Quantity**: 11028 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1093-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1093-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Internal Part Number: 3.9.; UDI/GTIN: 00887761985209; P2519NNC3A24 model number of impacted RubyTech Switch |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution to states of: NC and VA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: May 25, 2022
- **Recall initiation date**: Apr 13, 2022
- **Center classification date**: May 13, 2022
- **Termination date**: Dec 20, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1093-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Baxter Healthcare Corporation records](https://isitonrecall.com/brand/baxter-healthcare-corporation/)