HIGHFDA DEVICE

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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 8, 2025
Status
ACTIVE
Severity
7/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Securitas Healthcare
Product type
Call Station
Model numbers
CSK200-900MR
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 8, 2025

  2. Reported by FDA DEVICE

    January 14, 2026

  3. RecallRadar source check

    January 21, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

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.

Get instant alerts for Health & Personal Care recalls

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

No spamUnsubscribe anytime

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
  • 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

Taro Pharmaceuticals Withdraws Diclofenac Sodium Gel Over Viscosity Issues

Taro Pharmaceuticals announced a market withdrawal of Diclofenac Sodium, Topical Gel, 3% on January 27, 2026. The withdrawal stems from out of specification viscosity results. Healthcare providers and consumers should stop using the product immediately.

BEEKEEPER'S NATURALS USA
Microbial Contamination
Read more
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.

SUN PHARMACEUTICAL INDUSTRIES
Labeling: Not
Read more