# FDA recall Z-2417-2024

> **Securitas Healthcare LLC** · Class II · device recall initiated 2024-06-20.

## Product

Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.

## Reason for recall

There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.

## Distribution

US:  NE, MN, WA, MD, TX, ON, WI, OR, MS, CA, and Canada

## Key facts

- **Recall number:** Z-2417-2024
- **Recalling firm:** Securitas Healthcare LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-20
- **Report date:** 2024-07-31

- **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-2417-2024

## Citation

> AI Analytics. FDA recall Z-2417-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2417-2024. Source: US FDA. Licensed CC0.

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