FDA Device recall Z-0877-2013
QuietCare-Networked product, Facility Server/model: QC101601
- FDA Device
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of QuietCare-Networked product, Facility Server/model: QC101601 by Intel Ge Care Innovations, citing care Innovations detected a software anomaly: During the engineering investigation into the cause of why a Wander Alert was not generated, a defect in the implementation of the Wa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0877-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-12-16 |
| Published | 2013-03-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Intel Ge Care Innovations |
| Distribution | US |
Product
QuietCare-Networked product, Facility Server/model: QC101601; The QuietCare system is intended to detect and analyze residents' movements.
Reason
Care Innovations detected a software anomaly: During the engineering investigation into the cause of why a Wander Alert was not generated, a defect in the implementation of the Wander and Night Motion ADLs was discovered.
Identifiers
| code_info | All units of this model. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0877-2013%22
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