QuietCare-Networked — Class II medical device recall Z-1374-2013
Terminated recall by Intel-GE Care Innovations LLC, reported 2013-06-05. Customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.
| Recall number | Z-1374-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intel-GE Care Innovations LLC, Roseville, CA, United States |
| Recall initiated | 2013-04-04 |
| Classified | 2013-05-24 |
| Reported by FDA | 2013-06-05 |
| Terminated | 2013-06-04 |
| Countries outside the US | GB |
| Quantity | 46 |
Product
QuietCare-Networked. Intended for use in monitoring the environmental conditions and activity (motion) of an individual living in a senior housing community.
Reason for recall
Customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1374-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.