Lower riskMedical device recall · FDA · Published November 17, 2021
Stanley Senior Living Arial Emergency Systems: Memory Issues May Prevent Alarms
Stanley Security Solutions recalls Senior Living Arial emergency and nurse call systems with memory problems that could prevent alarms from working. Affected units have specific model and lot numbers listed in the recall notice.
“Stanley Senior Living Arial Emergency Systems: Memory Issues May Prevent Alarms.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61524-stanley-senior-living-arial-emergency-systems-memory-issues-may-prevent. Based on FDA recall #Z-0497-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0497-2022%22&limit=1).
Stanley Security Solutions Inc recalled Senior Living Arial Emergency and Nurse Call Systems due to failure to alarm, according to the FDA on Nov. 17, 2021. The recall covers systems with increased memory consumption issues.
How to tell if you have it
Brand: Stanley Security Solutions
Product: Senior Living Arial Emergency and Nurse Call Systems
Model No.: 0900-989
Lot Nos.: 7VQYZB3, G1GG8B3, 1TX2613, 7VQWZB3, GRRT243, 1TX3613, G1H58B3, HJP7N23, HJP9N23, 51SDR33, and GRRV243
UPC: 00840948100987
The hazard
The systems are not alarming due to increased memory consumption.
Context
GovInfoNow's records show Stanley Security Solutions Inc has two other recalls on record since Oct. 11, 2018. On June 14, 2019, the company recalled Arial 54315 Network Manager units due to outages traced to the Arial 54315 Serial-to-IP Network Gateway. Other recent recalls of similar products include Philips IntelliVue Multi Measurement Server X2 Recall (Oct. 31, 2025), Philips IntelliVue MP30 Monitor Recall (Oct. 31, 2025), and Philips IntelliVue MP5 Monitors May Not Alarm - Recall (Oct. 31, 2025).
How to tell if you have this one
Check for model numbers 0900-989 and lot numbers like 7VQYZB3, G1GG8B3, or 1TX2613. The recall includes specific units with unique UDI numbers starting with (01)00840948100987(21).
Brand
Stanley Security Solutions
Product
Senior Living Arial Emergency and Nurse Call Systems
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Model and Lot Numbers
Look for model number 0900-989 and lot numbers listed in the recall notice to confirm if your unit is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 7 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of FL, MD, MI, MN, SD, TN, and WA. The countries of Canada and Qatar.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Maryland, Michigan, Minnesota, South Dakota, Tennessee, Washington.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0497-2022 (November 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0497-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.