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Sign in to claim this brandSecuritas 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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- Phone
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- 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| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tek-Care Appliance Server, Page, 1 Ev Mon | NC475 | FDA UDI | Class II | Active |
| Ups 8-Outlet | PK250B | FDA UDI | Class II | Active |
| Arial | 52116 | FDA UDI | Class II | Active |
| Arial | CSK200 | FDA UDI | Class II | Active |
| Arial | 0900-240 | FDA UDI | Class II | Active |
| Dummy Plug, 1/4" Plastic - 5 Ea | JK018K | FDA UDI | Class II | Active |
| Arial | 2560-54337 | FDA UDI | Class II | Active |
| Arial | 14390-AUS | FDA UDI | Class II | Active |
| Arial U | 56106 | FDA UDI | Class II | Active |
| Tc120 Central Equipment Module, No Audio | NC120 | FDA UDI | Class II | Active |
| Network Switch, 8-Port | NC554/8 | FDA UDI | Class II | Active |
| Kit, Panel, Pl691, 5-Pcs | RP131K | FDA UDI | Class II | Active |
| Fall monitor | 93030 | FDA UDI | Class I | Active |
| Fall monitor | 26201AS | FDA UDI | Class I | Active |
| STANLEY Healthcare | TAG-P1000 | FDA UDI | Class II | Active |
| Fall monitor | 26201 | FDA UDI | Class I | Active |
| Arial | 0900-652 | FDA UDI | Class II | Active |
| Arial | 52114 | FDA UDI | Class II | Active |
| M200 Fall Monitor | M200 | FDA UDI | Class I | Active |
| BED PAD, 10x30, 90-DAY, 8FT, TABS | 26100 | FDA UDI | Class I | Active |
| Arial | 59364 | FDA UDI | Class II | Active |
| Call Cord 6 Ft, 1/4" Plug, Geriatric Oxy Safe | SF301G | FDA UDI | Class II | Active |
| Arial | CSK200-1069 | FDA UDI | Class II | Active |
| Dlx. Bed Monitor W/45 Day Pad | 95780 | FDA UDI | Class I | Unknown |
| Bed Pad, 180day, 6 Pack, Bsm-2b-6 | 95100 | FDA UDI | Class I | Active |
| UMP Sentry Kit with 45-Day Bed Pad | 97100 | FDA UDI | Class I | Active |
| Arial | 2560-59362R | FDA UDI | Class II | Active |
| M200-C Fall Monitor (M200 With Closed Battery Compartment Cover) | M200-C | FDA UDI | Class I | Active |
| Securitas Healthcare | 75000 | FDA UDI | Class I | Active |
| Arial | 54330 | FDA UDI | Class II | Active |
| Arial | 54311 | FDA UDI | Class II | Active |
| Paging Transmitter 2 Port | NC365B | FDA UDI | Class II | Active |
| Arial | CSK200-900MR | FDA UDI | Class II | Active |
| Central Equip, 6 Mstr, 64 Stn, Audio, Tc160 | NC160 | FDA UDI | Class II | Active |
| CHAIR PAD, 7x15, 45-DAY, 8FT, ANTI-SLIP | 93010AS | FDA UDI | Class I | Active |
| Arial | 2560-55352 | FDA UDI | Class II | Active |
| Arial | 2560-54321 | FDA UDI | Class II | Active |
| STANLEY Healthcare | CSK-1000-MR | FDA UDI | Class II | Active |
| Wall Mount Bracket, Nc415av | IH415W | FDA UDI | Class II | Active |
| Arial | 2560-59360R | FDA UDI | Class II | Active |
| Monitor, Pro, Tabs W/Plastic Bkt & Reset, Ce | 25222CE | FDA UDI | Class I | Unknown |
| Single Room Station, 1/4"jk, Tc120 | SF121 | FDA UDI | Class II | Active |
| Custom 2-Button Pull-Cord Station, Tc120 | SF123 | FDA UDI | Class II | Active |
| Arial U | 56112 | FDA UDI | Class II | Active |
| Arial | 54305 | FDA UDI | Class II | Active |
| CHAIR PAD, 7x15, 14-DAY, 4FT, TABS | 26200 | FDA UDI | Class I | Active |
| Bed Pad, 45day, 6 Pack, Bsm-1w-6 | 95080 | FDA UDI | Class I | Active |
| Arial | 54350 | FDA UDI | Class II | Active |
| Arial | 0900-241 | FDA UDI | Class II | Active |
| Arial | 2560-55365 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 8, 2025 | Z-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, 2025 | Z-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, 2024 | Z-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, 2024 | Z-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, 2024 | Z-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, 2024 | Z-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, 2023 | Z-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, 2023 | Z-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, 2023 | Z-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, 2023 | Z-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. |