The Recall Desk
HighFDA (Devices)·Z-0220-2024·Announced 2023-11-15

Arial Water Resistant Pendant Alarm Recalled for Battery Depletion Risk

Securitas Healthcare is recalling Arial Water Resistant Pendants (models 59360 and 2560-59360) due to premature battery depletion that may prevent emergency alarms from being received.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II recall of a patient alarm device where premature battery depletion may prevent emergency alerts from being received. No reported injuries or illnesses. Rated High per rubric criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Securitas Healthcare LLC is recalling the Arial Water Resistant Pendant with Neck Lanyard, a mobile patient alarm system (models 59360 and 2560-59360). Approximately 1,235 units with manufacturing date codes 23128 to 23251 are affected by this recall.

The recalled pendants may experience premature battery depletion, which presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.

The affected units have been distributed worldwide, including throughout the United States and Canada. Consumers who own these devices should contact Securitas Healthcare LLC for information about the recall.

The recalled product

Product
Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; mobile patient alarm
Manufacturer
Securitas Healthcare LLC
Hazard
  • battery-depletion
  • alarm-failure

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Manufacturing date codes: 23128 to 23251

Distribution

Distributed nationwide across the United States.