Arial 54600Recalls & reported problems
Securitas Healthcare LLC · Arial Mobile App · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 11, 2024Open, 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.
Z-1943-2024 · Root cause: Under Investigation by firm · FDA record ↗
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- GEN4 INTERACTIVE 4Z19EE-Z100038Curbell Medical Products, Inc. · System, Environmental Control, Powered3 reports
- GEN4 INTERACTIVE 4M380E-Z103018Curbell Medical Products, Inc. · System, Environmental Control, Powered2 reports
- GEN4 INTERACTIVE 412400N-0300018Curbell Medical Products, Inc. · System, Environmental Control, Powered2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.