RegWardenFDA facility compliance records
Recall

Class II — Securitas Healthcare LLC

Recalling firmSecuritas Healthcare LLC.
Registered facilityAeroScout, Ltd. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonSecuritas 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.
ProductArial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
Quantity1898 units
DistributionWorldwide distribution -US Nationwide and the country of Canada.
Initiated2025-12-08
Classified2026-01-08
Recall numberZ-1032-2026
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Securitas Healthcare LLC (Z-1032-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98122/

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