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

Recall Insight

This FDA Devices action (record #Z-0221-2024) was formally reported on November 15, 2023, with the manufacturer initiating the action on September 25, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Securitas Healthcare LLC is listed as the recalling firm, operating out of Lincoln, NE. Federal records indicate 2691 units units are affected.

The documented reason for this recall is: Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System. Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide and the country of Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 3 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.