Recall Z-0220-2024— Securitas Healthcare LLC
Class II · Ongoing
Class II FDA medical device recall by Securitas Healthcare LLC, initiated 2023-09-25. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Securitas Healthcare LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-09-25
- Firm location
- Lincoln, NE, United States
Product description
Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; 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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.