HIGH

Securitas Healthcare Recalls 900 MHz Call Station Over Battery Alert Failure

Securitas Healthcare recalled 1,898 units of the Arial 900 MHz Call Station on December 8, 2025. A firmware issue may prevent low battery alerts, posing a risk of battery failure. Users should stop using the device immediately and follow recall instructions.

Quick Facts at a Glance

Recall Date
December 8, 2025
Hazard Level
HIGH
Brand
Securitas Healthcare
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Securitas Healthcare LLC or your healthcare provider for instructions. Notification method: Letter

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

The Arial 900 MHz Call Station is used in healthcare settings for emergency communication. It allows users to alert healthcare staff in case of emergencies, making it crucial for patient safety.

Why This Is Dangerous

The firmware issue prevents timely low battery alerts, which could lead to the device failing when needed most. This poses a significant risk in emergency situations.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Users of the affected Call Stations may be left without critical emergency communication if the battery fails unexpectedly.

Practical Guidance

How to identify if yours is affected

  1. Check the model number: CSK200-900MR
  2. Verify the firmware version: 1.6.3
  3. Inspect the purchase date to ensure it falls between January 1, 2023, and June 26, 2024.

Where to find product info

The model number and firmware version are typically located on the bottom or back of the device.

What timeline to expect

Expect a refund processing timeline of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Contact Securitas Healthcare again via phone or email.
  • Document all correspondence attempts.
  • Consider filing a complaint with the CPSC if there is no response.

How to prevent similar issues

  • Look for medical devices with robust safety certifications.
  • Research product reviews focusing on reliability and safety features.
  • Ensure any medical alert system has a clear battery life indicator.

Documentation advice

Keep records of all communications, return receipts, and any photos of the product for your documentation.

Product Details

The recalled product is the Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version 1.6.3. These devices were sold between January 1, 2023, and June 26, 2024, with a total quantity of 1,898 units distributed worldwide, including the U.S. and Canada.

Key Facts

  • Recalled model: CSK200-900MR
  • Firmware version: 1.6.3
  • Quantity: 1,898 units
  • Worldwide distribution including U.S. and Canada

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
CSK200-900MR
Affected States
ALL
Report Date
January 14, 2026
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
MEDIUM

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

LACTATED RINGERS
Presence of
Read more
Recalled ZOLIQUEX Bed Rail (front view)
HIGH

ZOLIQUEX Adult Portable Bed Rails Recalled for Entrapment, Asphyxiation Risk (2026)

ZOLIQUEX recalled adult portable bed rails sold on Amazon after reports of entrapment and asphyxiation risk. The recall targets silver bed rails measuring 12.4 inches wide by 33.07 inches tall and weighing 7.1 pounds. The model numbers ZEX014-V1 and the Zoliquex branding appear on packaging. Stop using the product and seek a full refund by contacting ZOLIQUEX.

ZOLIQUEX, of China
The recalled
Read more
Recalled Arey, Not Today, Grey (180ct) - front
HIGH

Vitaquest International Recalls Multiple Iron Supplements for Child-Resistant Packaging Violations (

Vitaquest International recalled Arey Not Today iron supplements sold at retailers nationwide after determining the products do not meet the Poison Prevention Packaging Act's child-resistant packaging requirement. The noncompliant packaging creates a poisoning risk to young children if ingested. Consumers should stop using the products immediately and contact Vitaquest for a free child-resistant替换

Vitaquest International LLC of West Caldwell, New Jersey
The dietary
Read more
Recalled Easymake Bed Rail
HIGH

Easymake Adult Portable Bed Rails Recalled for Entrapment Risk (2026)

Easymake adult portable bed rails imported by ZFZG-US are recalled on April 9, 2026. The recall cites a risk of entrapment and asphyxiation and notes the product lacks required hazard warning labels. Stop using the recalled rails immediately and contact ZFZG-US for a full refund.

Zhongshan Yungu Daily Products, of China
The recalled
Read more
Recalled Tuymec Minoxidil Hair Growth Serum Spray Bottle (front and back)
HIGH

Tuymec Minoxidil Hair Growth Kit Recalled for Non-Child-Resistant Packaging (2026)

Tuymec Minoxidil Hair Growth Kit sold on Amazon by DrHealBeauty is recalled for non-child-resistant packaging. The kit contains two black spray bottles with 5% minoxidil and BIOTIN labels. Consumers should stop using the product immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure.

Tuymec Minoxidil Hair Growth Spray Bottles
The hair
Read more
Recalled TecFlox Topical Solution - hair and beard growth serum bottle
HIGH

TecFlox Minoxidil Topical Solution Hair Serum Recalled for Child Poisoning Risk (2026)

TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of

TecFlox Hair and Beard Growth Serum Bottles
The hair
Read more