Arial recallZ-1250-2023 · Securitas Healthcare LLC · initiated Feb 6, 2023
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Securitas Healthcare LLC or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.
FDA root cause category: Under Investigation by firm
What the company is doing
The recalling firm issued letters dated 1/24/2023 on 2/6/2023 via certified mail to the potentially impacted clients. The letters described the issue and informed the client this only applies to those versions of Arial Mobile Application v11.0.0.2 for Android devices downloaded from the Google Play Store and does not apply to versions received directly from Securitas Healthcare. It also does not apply to mobile devices with an iOS operating system. The letter explains that the client will be unable to use the Arial Mobile Application and will not receive or be able to view and respond to notifications and system warnings on their Android devices. For the clients who have already upgraded their Android devices to Arial Mobile Application v11.0.0.2 for Android from the Google Play Store, they are to contact the Securitas Healthcare Technical Support Team for instructions on how to obtain and install a working version of the application for Android devices. In the interim, they are to use the Arial Server or Arial Web Client to view and respond to notifications and system warnings. For clients who have not yet updated to the affected version, they may continue to use the previous unaffected version. They are instructed: (1) to not download or upgrade to the affected version from the Google Play store; (2) set the Mobile Device Management package to not push Arial Mobile Application v11.0.0.2 updates automatically; (3) inform staff and caregivers not to download or install the affected version; and (4) to disable automatic updates on their Android devices. All clients are to disseminate the notice to all affected areas within their facility and satellite facilities which may be using the mobile application and the clients are to complete the attached response form, even if their facility does not use the mobile application. The response form indicates whether or not the facility uses this application and has notified all affected parties.
Recall details
- Recall number
- Z-1250-2023
- Status
- Open, Classified
- Initiated by the company
- Feb 6, 2023
- Posted by the FDA
- Mar 14, 2023
- Recalling firm
- Securitas Healthcare LLC
- Quantity
- Approximately 350 downloads
- Product code
- IQA
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
Product description
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Code information (models, lots, serial numbers)
v11.0.0.2 downloaded from the Google Play Store on or after 1/14/2023, UDI (01)00840948102769(10)110026.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- ARIAL 54305Securitas Healthcare LLC · System, environmental control, powered1 recall0 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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