Room Controller, Univ. Dome LT., TC120

Catalogue number LI122UN, listed by Securitas Healthcare LLC, United States, under System, Environmental Control, Powered. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
12recalls on this code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code IQA
Manufacturer City Province Registered as Device types
Yuiyn HOO Industrial Limited Dong Guan Guangdong Contract manufacturer 3

Record

Regulatory record for Room Controller, Univ. Dome LT., TC120
Listed by Securitas Healthcare LLC, United States
FDA product code IQA
Device type System, Environmental Control, Powered
Device class Class 2
Regulation 21 CFR 890.3725
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2021-12-07
Record revised 2024-02-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Room Controller, Univ. Dome LT., TC120
Catalogue number Size Status
LI122UN In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GEN4 Digital Curbell Medical Products, Inc. 922
GEN4 Interactive Curbell Medical Products, Inc. 456
GEN4 Plus, Direct Access Curbell Medical Products, Inc. 142
Arial Securitas Healthcare LLC 96
Ascom Ascom Sweden AB 77
Elite Digital Crest Healthcare Supply 71
Amplion Care Assurance Amplion Clinical Communications, Inc. 67
Elite Infrared Crest Healthcare Supply 59
Responder 5, Standard Curbell Medical Products, Inc. 33
Excel Digital Crest Healthcare Supply 28
Responder 5, Standard,no Entertainment Curbell Medical Products, Inc. 28
Excel EntertainIR Crest Healthcare Supply 24

Showing 12 of 819. All products under System, Environmental Control, Powered

Recalls

12 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2025-12-08 Class II Under Investigation by firm 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 1898 units
2025-12-08 Class II Under Investigation by firm 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 5627 units
2024-11-01 Class II Software Design Change Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System. 111 systems
2024-06-20 Class II Software Manufacturing/Software Deployment There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery. 1268 units
2024-06-20 Class II Software Manufacturing/Software Deployment This is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery. 77 units
2024-04-11 Class II Under Investigation by firm 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 661 sites with mobile application user licenses
2023-09-25 Class II Component change control Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System. 2691 units
2023-09-25 Class II Component change control Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System. 1235 units
2023-09-25 Class II Component change control Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System. 49 devices
2023-02-06 Class II Under Investigation by firm The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices. Approximately 350 downloads
2021-11-17 Class II Component design/selection Systems are not alarming due to increased memory consumption. 11 units (systems)
2019-06-14 Class II Under Investigation by firm STANLEY Healthcare has received reports of outages on the Arial nurse call system. These outages have been traced back to the Arial 54315 Serial-to-IP Network Gateway. 137 units 2021-05-13

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer