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Securitas Healthcare LLC

US

Last updated September 17, 2026

What Securitas Healthcare LLC makes

Securitas Healthcare LLC manufactures patient safety and communication devices for home and ambulatory care, including fixed and ambulatory call buttons, nurse call systems, fall sensors, and medical networking interfaces. Their product line also covers home alert systems for vulnerable patients, pager/phone solutions, and mounting accessories like chair pads and floor mats.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated under US medical device standards, with products intended for use in healthcare settings to enhance patient monitoring and emergency response.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
4600 Vine St, LINCOLN, NE, 68503
Website
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LinkedIn
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Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
1929691
DUNS Number
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Catalogue (211)

Page 4 of 5
DeviceModel / ReferenceRegistriesClassStatus
Tek-Care Appliance Server, Page, 1 Ev Mon NC475
FDA UDI
Class IIActive
Ups 8-Outlet PK250B
FDA UDI
Class IIActive
Arial 52116
FDA UDI
Class IIActive
Arial CSK200
FDA UDI
Class IIActive
Arial 0900-240
FDA UDI
Class IIActive
Dummy Plug, 1/4" Plastic - 5 Ea JK018K
FDA UDI
Class IIActive
Arial 2560-54337
FDA UDI
Class IIActive
Arial 14390-AUS
FDA UDI
Class IIActive
Arial U 56106
FDA UDI
Class IIActive
Tc120 Central Equipment Module, No Audio NC120
FDA UDI
Class IIActive
Network Switch, 8-Port NC554/8
FDA UDI
Class IIActive
Kit, Panel, Pl691, 5-Pcs RP131K
FDA UDI
Class IIActive
Fall monitor 93030
FDA UDI
Class IActive
Fall monitor 26201AS
FDA UDI
Class IActive
STANLEY Healthcare TAG-P1000
FDA UDI
Class IIActive
Fall monitor 26201
FDA UDI
Class IActive
Arial 0900-652
FDA UDI
Class IIActive
Arial 52114
FDA UDI
Class IIActive
M200 Fall Monitor M200
FDA UDI
Class IActive
BED PAD, 10x30, 90-DAY, 8FT, TABS 26100
FDA UDI
Class IActive
Arial 59364
FDA UDI
Class IIActive
Call Cord 6 Ft, 1/4" Plug, Geriatric Oxy Safe SF301G
FDA UDI
Class IIActive
Arial CSK200-1069
FDA UDI
Class IIActive
Dlx. Bed Monitor W/45 Day Pad 95780
FDA UDI
Class IUnknown
Bed Pad, 180day, 6 Pack, Bsm-2b-6 95100
FDA UDI
Class IActive
UMP Sentry Kit with 45-Day Bed Pad 97100
FDA UDI
Class IActive
Arial 2560-59362R
FDA UDI
Class IIActive
M200-C Fall Monitor (M200 With Closed Battery Compartment Cover) M200-C
FDA UDI
Class IActive
Securitas Healthcare 75000
FDA UDI
Class IActive
Arial 54330
FDA UDI
Class IIActive
Arial 54311
FDA UDI
Class IIActive
Paging Transmitter 2 Port NC365B
FDA UDI
Class IIActive
Arial CSK200-900MR
FDA UDI
Class IIActive
Central Equip, 6 Mstr, 64 Stn, Audio, Tc160 NC160
FDA UDI
Class IIActive
CHAIR PAD, 7x15, 45-DAY, 8FT, ANTI-SLIP 93010AS
FDA UDI
Class IActive
Arial 2560-55352
FDA UDI
Class IIActive
Arial 2560-54321
FDA UDI
Class IIActive
STANLEY Healthcare CSK-1000-MR
FDA UDI
Class IIActive
Wall Mount Bracket, Nc415av IH415W
FDA UDI
Class IIActive
Arial 2560-59360R
FDA UDI
Class IIActive
Monitor, Pro, Tabs W/Plastic Bkt & Reset, Ce 25222CE
FDA UDI
Class IUnknown
Single Room Station, 1/4"jk, Tc120 SF121
FDA UDI
Class IIActive
Custom 2-Button Pull-Cord Station, Tc120 SF123
FDA UDI
Class IIActive
Arial U 56112
FDA UDI
Class IIActive
Arial 54305
FDA UDI
Class IIActive
CHAIR PAD, 7x15, 14-DAY, 4FT, TABS 26200
FDA UDI
Class IActive
Bed Pad, 45day, 6 Pack, Bsm-1w-6 95080
FDA UDI
Class IActive
Arial 54350
FDA UDI
Class IIActive
Arial 0900-241
FDA UDI
Class IIActive
Arial 2560-55365
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (10)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Securitas Healthcare LLC has initiated 10 recall records between February 6, 2023, and December 8, 2025, with records currently marked as either open or classified. The recalls involve issues with software, firmware, and mobile application functionality, including failures in user notifications, alarm transmission delays, battery depletion risks, and compatibility problems with Android and iOS devices (specifically versions 17.4 and 17.5). The reasons cited relate to non-compliance with specified performance standards and potential operational disruptions in emergency and nurse call systems.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Dec 8, 2025Z-1032-2026—open, classified

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.

Dec 8, 2025Z-1031-2026—open, classified

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.

Nov 1, 2024Z-0570-2025—open, classified

Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.

Jun 20, 2024Z-2418-2024—open, classified

This is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery.

Jun 20, 2024Z-2417-2024—open, classified

There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.

Apr 11, 2024Z-1943-2024—open, classified

The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is frequently restarting causing the app to receive alerts for all pending alarm notifications and other events when the app restarts, experience difficulty in placing and maintaining staff-to-staff phone calls, and frequently appears offline while the app restarts.

Sep 25, 2023Z-0222-2024—open, classified

Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.

Sep 25, 2023Z-0220-2024—open, classified

Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.

Sep 25, 2023Z-0221-2024—open, classified

Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.

Feb 6, 2023Z-1250-2023—open, classified

The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.