FDA Device recall Z-1375-2013
QuietCare
- FDA Device
- Class II
- terminated
- Published 2013-06-05
On 2013-06-05 the FDA classified a Class II recall of QuietCare by Intel Ge Care Innovations, citing customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1375-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-04 |
| Published | 2013-06-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Intel Ge Care Innovations |
| Distribution | n/a |
Product
QuietCare. Intended for use in monitoring the environmental conditions and activity (motion) of an individual living in a senior housing community.
Reason
Customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.
Identifiers
| code_info | US QuietCare: QC200403, v.02; QC200403, v.03; QC200403, v.04; QC200405 UK QuietCare: QCE200403, v.02; QCE200403, v.03 |
|---|
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-1375-2013%22
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