The Recall Desk
HighFDA (Devices)·Z-0497-2022·Announced 2022-01-26

Senior Living Nurse Call Systems Failing to Alarm Due to Memory Issue

Stanley Security Solutions is recalling 11 Senior Living Arial Emergency and Nurse Call Systems because they fail to alarm due to increased memory consumption, potentially preventing nursing staff from responding to resident emergencies.

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: This is an FDA Class II recall of a risk-of-harm product—an emergency alert system that fails to function properly. Although no illnesses or injuries have been reported, the potential for harm is significant because these systems are critical for summoning emergency assistance in senior living facilities.

Plain-English summary

Stanley Security Solutions Inc. is recalling 11 Senior Living Arial Emergency and Nurse Call Systems (Model No. 0900-989). These systems are used in senior living facilities to alert staff when residents need emergency assistance.

The systems fail to alarm due to increased memory consumption. When a resident activates an emergency call button, the system does not properly notify nursing staff. This could delay emergency response when assistance is needed.

The recalled systems were distributed nationwide in Florida, Maryland, Michigan, Minnesota, South Dakota, Tennessee, and Washington, as well as in Canada and Qatar. Additional information about the affected lot numbers and recall details is available from the manufacturer and the FDA.

The recalled product

Product
Senior Living Arial Emergency and Nurse Call Systems
Manufacturer
Stanley Security Solutions Inc
Category
Medical Device — Emergency / Nurse Call System
Hazard
  • 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 (20)

  • Model No. 0900-989
  • Lot No.: 7VQYZB3
  • G1GG8B3
  • 1TX2613
  • 7VQWZB3
  • GRRT243
  • 1TX3613
  • G1H58B3
  • HJP7N23
  • HJP9N23
  • 51SDR33
  • and GRRV243
  • UDI No.: (01)00840948100987(21)7VQYZB3
  • (01)00840948100987(21)1TX2613
  • (01)00840948100987(21)7VQZZB3
  • (01)00840948100987(21)GRRT243
  • (01)00840948100987(21)G1GF8B3
  • (01)00840948100987(21)1TX3613
  • (01)00840948100987(21)G1H58B3
  • (01)00840948100987(21)HJP7N23

Distribution

Distributed nationwide across the United States.

Related recalls

Same category