Z-1250-2023 Class II Ongoing
FDA device recall Z-1250-2023 was initiated by Securitas Healthcare LLC on February 6, 2023 and is designated Class II. Reason for recall: The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices. The recall status is ongoing. Affected quantity: Approximately 350 downloads.
Recall Details
- Product Type
- Devices
- Report Date
- March 22, 2023
- Initiation Date
- February 6, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- Approximately 350 downloads
Product Description
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Reason for Recall
The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.
Distribution Pattern
Worldwide distribution - US Nationwide and the country of Canada.
Code Information
v11.0.0.2 downloaded from the Google Play Store on or after 1/14/2023, UDI (01)00840948102769(10)110026.