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GEN4 INTERACTIVE

CURBELL MEDICAL PRODUCTS, INC. · Model 414190E-0100038 · UDI-DI 00840828126199

IQA
10
510(k) clearances
37
Adverse events (4 deaths)
17
Recalls
18
Facilities

Description

GEN4 INTERACTIVE

Recalls

DateFirmReason
2025-12-08Securitas Healthcare LLCSecuritas 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 batt
2025-12-08Securitas Healthcare LLCSecuritas 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 batt
2024-11-01Securitas Healthcare LLCCertain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.
2024-06-20Securitas Healthcare LLCThis is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery.
2024-06-20Securitas Healthcare LLCThere is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
2024-04-11Securitas Healthcare LLCThe 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
2023-09-25Securitas Healthcare LLCPremature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
2023-09-25Securitas Healthcare LLCPremature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
2023-09-25Securitas Healthcare LLCPremature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
2023-02-06Securitas Healthcare LLCThe mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.