Securitas Healthcare LLC: Device Recall

Recall #Z-2418-2024 · 06/20/2024

Class II: Risk

Recall Details

Recall Number: Z-2418-2024
Classification: Class II
Product Type: Device
Recalling Firm: Securitas Healthcare LLC
Status: Ongoing
Date Initiated: 06/20/2024
Location: Lincoln, NE, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 77 units

Reason for Recall

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

Product Description

Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.

Distribution Pattern

US: FL, CA, AL, ND, MS, WA, MN, TX, OR, WI, MD, NY, NE

Other Recalls by Securitas Healthcare LLC

Class II: Risk 12/08/2025

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.
Class II: Risk 12/08/2025

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.
Class II: Risk 11/01/2024

Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.
Class II: Risk 06/20/2024

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

View all recalls by Securitas Healthcare LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.