PlainRecalls
FDA Devices Moderate Class II Ongoing

Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm

Reported: November 15, 2023 Initiated: September 25, 2023 #Z-0221-2024

Product Description

Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm

Reason for Recall

Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.

Details

Recalling Firm
Securitas Healthcare LLC
Units Affected
2691 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Location
Lincoln, NE

Frequently Asked Questions

What product was recalled?
Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm. Recalled by Securitas Healthcare LLC. Units affected: 2691 units.
Why was this product recalled?
Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 15, 2023. Severity: Moderate. Recall number: Z-0221-2024.