Device recalls

Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the Ar…

Securitas Healthcare LLC · 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 notificatio…

Open, ClassifiedUnder Investigation by firmZ-1943-2024
Open FDA's page for this record
Cfres ID
207714
Product res number
Z-1943-2024
Event date initiated
2024-04-11
Event date posted
2024-05-31
Recall status
Open, Classified
Res event number
94607
Product code
IQA
Code info
Arial Mobile v11.0.0 UDI: (01)00840948100963(10)1100.
Firm FEI number
1929691
Recalling firm
Securitas Healthcare LLC
Address 1
4600 Vine St
City
Lincoln
State
NE
Postal code
68503-2823
Additional info contact
Ameya Oke 812-371-7115
Root cause description
Under Investigation by firm
Product quantity
661 sites with mobile application user licenses
Distribution pattern
Worldwide distribution - US Nationwide and the countries of Australia, Canada, England, Hong Kong, France, Qatar, and Spain.
Product description

Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the Arial Emergency and Nurse Call System.

Reason for recall

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.

Action

Phone calls were initiated on 4/11/2024 and the sales teams used the information in a FAQ document during the call. The FAQ explained what happened, what products are affected, the potential hazards, whether the application will still be operational, what to do if the customer has or has not upgraded their operating system to Apple iOS 17.4 or later, can the Arial Server or workstations still be used effectively, does the issue affect Android mobile devices, does the issue affect any other functionality of Arial Emergency and Nurse Call System, who can the customer contact for more information, and when will the update be available. Recall letters were dated and issued on 4/11/2024 via certified mail. The letter described the issue, informed the customer this communication does not apply to users using mobile devices with an Android operating system, provided information on the affected product, the hazard involved, and the necessary actions to take. The actions were: 1. For users that have not already upgraded their mobile devices utilizing Apple iOS 17.3 or earlier to Apple iOS 17.04 or Apple iOS 17.5, the customer should not upgrade their operating system and disable automatic updates. 2. For clients that have already upgraded their mobile device operating system to Apple iOS 17.4, they were informed there is no current mitigation to the issue and the recalling firm is working to identify and develop a mitigation and permanent solution. Alerts for alarms and other events will continue to be received by the Arial Server and Arial workstations. In the interim, Securitas Healthcare suggests that users use the Arial Server or Arial workstations to view and respond to notifications and system warnings. Users with Apple iOS 17.4 were instructed to not upgrade their operating system to Apple iOS 17.5 and disable automatic updates. Instructions were enclosed on disabling automatic updates. 3. For users that have already upgraded their mobile device operati

Harmonized identifiers (openFDA)
Device name
System, Environmental Control, Powered
Medical specialty description
Physical Medicine
Regulation number
890.3725
Device class
2
K number
K943244, K911101, K851740, K944585, K850314, K902664, K901028, K953905, K944345, K873612, K840808, K850313, K900969, K770028, K872937, K832057, K926029, K881634, K890596, K872936, K940223, K921528, K953937, K961306
Registration number
1929691, 3014024339, 3012505893, 3003114240, 3030181825, 3002713667, 3009591865, 1320360, 3013513594, 3006802317, 3011699327, 3017404332, 3007200970, 3008952681, 3001757821, 3006789226, 3008855170, 3021667368
FEI number
1929691, 3014024339, 3012505893, 3000210521, 3003114240, 3030181825, 3002713667, 3009591865, 3013513594, 3011699327, 3006802317, 3017404332, 3007200970, 3008952681, 3001757821, 3006789226, 3008855170, 3021667368
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.