FDA Device recall Z-0220-2024
Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360
- FDA Device
- Class II
- ongoing
- Published 2023-11-15
On 2023-11-15 the FDA classified a Class II recall of Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360 by Securitas Healthcare, citing premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0220-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-25 |
| Published | 2023-11-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Securitas Healthcare |
| Distribution | US |
Product
Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; mobile patient alarm
Reason
Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
Identifiers
| code_info | Manufacturing date codes: 23128 to 23251 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0220-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.