Class II — Securitas Healthcare LLC
| Recalling firm | Securitas Healthcare LLC. |
|---|---|
| Registered facility | AeroScout, Ltd. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System. |
| Product | Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm |
| Quantity | 2691 units |
| Distribution | Worldwide distribution - US Nationwide and the country of Canada. |
| Initiated | 2023-09-25 |
| Classified | 2023-11-03 |
| Recall number | Z-0221-2024 |
| Initiation | Voluntary: 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-0221-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93188/
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