---
title: "Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery... — FDA record Z-2417-2024 | Is It on Recall"
description: "There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery."
url: https://isitonrecall.com/recall/fda-device-z-2417-2024-arial-call-station-model-numbers-csk200-and-csk200mr-is-a-wireless-battery-operated-call-device-inst/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside r... — FDA record Z-2417-2024

Reported ongoing

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 Jun 20, 2024. 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**: 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**: There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
- **Classification**: Class II
- **Recalling firm**: Securitas Healthcare LLC
- **Quantity**: 1268 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2417-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2417-2024%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 | All units of the Affected Device Models sold between July 26, 2022 and June 5, 2024 |

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

## Distribution

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

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

- [California](https://isitonrecall.com/state/california/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Jul 31, 2024
- **Recall initiation date**: Jun 20, 2024
- **Center classification date**: Jul 23, 2024

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-2417-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Securitas Healthcare LLC records](https://isitonrecall.com/brand/securitas-healthcare-llc/)