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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/Home Healthcare

Securitas Healthcare LLC: Arial Patient Alarms Recalled for Premature Battery Depletion

Agency Publication Date: November 3, 2023
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Summary

Securitas Healthcare LLC is recalling approximately 3,975 Arial Water Resistant Pendants, which are mobile patient alarms used to signal for help. The affected models include the Neck Lanyard, Wristband, and Long Wristband versions (Models 59360, 59361, 59362 and their 2560-series equivalents). These devices are being recalled because the batteries may drain faster than expected, potentially causing the device to fail when a patient needs to send an emergency signal. These pendants were distributed worldwide, including throughout the United States and Canada, with manufacturing date codes ranging from 23128 to 23251.

Risk

If the battery depletes prematurely, the pendant may not have enough power to send a signal to the Arial Wireless Emergency Call System. This means that if a patient presses the button during an emergency, the alarm will not be received by healthcare staff, potentially leading to a delay in critical medical assistance.

What You Should Do

  1. Identify if you have an affected Arial Water Resistant Pendant by checking the model number and manufacturing date code on the device. Affected models include 59360, 2560-59360 (Neck Lanyard); 59361, 2560-59361 (Wristband); and 59362, 2560-59362 (Long Wristband).
  2. Verify the manufacturing date code on your device: the recall specifically impacts units with codes ranging from 23128 to 23251.
  3. If your device matches the affected models and date codes, contact your healthcare provider or Securitas Healthcare LLC immediately to report the affected units and receive instructions on mitigation or replacement.
  4. Healthcare facilities should monitor the battery status of these devices closely and ensure a system is in place for alternative emergency signaling if a device fails.
  5. For further information or to discuss a potential remedy, contact Securitas Healthcare LLC at their headquarters located at 4600 Vine St, Lincoln, Nebraska.
  6. For additional questions regarding this recall, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer notification and guidance

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Arial Water Resistant Pendant with Neck Lanyard
Model / REF:
59360
2560-59360
Lot Numbers:
Manufacturing date codes: 23128 to 23251
Product: Arial Water Resistant Pendant with Wristband
Model / REF:
59361
2560-59361
Lot Numbers:
Manufacturing date codes: 23128 to 23251
Product: Arial Water Resistant Pendant with Long Wristband
Model / REF:
59362
2560-59362
Lot Numbers:
Manufacturing date codes: 23128 to 23251

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93188
Status: Active
Manufacturer: Securitas Healthcare LLC
Sold By: Securitas Healthcare LLC; Healthcare facilities
Manufactured In: United States
Units Affected: 3 products (1235 units; 2691 units; 49 devices)
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.