# FDA recall Z-1032-2026

> **Securitas Healthcare LLC** · Class II · device recall initiated 2025-12-08.

## Product

Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3

## Reason for recall

Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.

## Distribution

Worldwide distribution -US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-1032-2026
- **Recalling firm:** Securitas Healthcare LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-08
- **Report date:** 2026-01-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lincoln, NE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1032-2026

## Citation

> AI Analytics. FDA recall Z-1032-2026. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-1032-2026. Source: US FDA. Licensed CC0.

---

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