# FDA recall Z-1306-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-05-31.

## Product

NaviCare Nurse Call/Voalte Nurse Call

## Reason for recall

An issue has been identified with Phillips (Emergin) and Longleaf non relay (Connexall, Vocera, Cerner) wireless integrations used with NaviCare/Voalte Nurse Call, software versions 3.9.100 through 3.9.300. Calls placed from a push button call device, such as a push button switch, call cord, or from the push buttons on a room audio station, will be canceled on the nurse call system when the call is answered at the wireless phone, regardless of the call priority.

## Distribution

nationwide and Canada

## Key facts

- **Recall number:** Z-1306-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-31
- **Report date:** 2022-07-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1306-2022

## Citation

> AI Analytics. FDA recall Z-1306-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1306-2022. Source: US FDA. Licensed CC0.

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