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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Monitoring Devices

Arial Server Software Recalled for Emergency Call Notification Failure

Agency Publication Date: November 27, 2024
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Summary

Securitas Healthcare LLC has recalled 111 systems of its Arial Server Software, specifically versions 11.1.4 through 11.1.6 (SKU 54305). This software, which is used in hospitals and care facilities alongside the Arial Mobile and Arial Care Giver applications, may fail to alert staff when a patient or resident triggers an emergency or nurse call. Although no injuries have been reported, facility administrators should contact the manufacturer immediately to coordinate a software correction or update.

Risk

The software defect prevents emergency call notifications from reaching staff devices, potentially causing dangerous delays in medical response. If a patient experiences a medical crisis and the call is not received, it could lead to serious injury or death.

What You Should Do

  1. The recalled products are Arial Server Software versions 11.1.4 through 11.1.6 (SKU 54305) used in conjunction with the Arial Mobile Application or Arial Care Giver Application.
  2. Stop using the recalled software. Contact Securitas Healthcare LLC or your authorized distributor to arrange for a software update, replacement, or correction.
  3. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for more information regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Arial Server Software Versions 11.1.4 through 11.1.6 (111 systems)
Model / REF:
SKU 54305

Affected when used in conjunction with the Arial Mobile Application or Arial Care Giver Application; Includes versions 11.1.4, 11.1.5, and 11.1.6.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95652
Status: Active
Manufacturer: Securitas Healthcare LLC
Sold By: Securitas Healthcare LLC
Manufactured In: United States
Units Affected: 111 systems
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.