Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1375-2013 — QuietCare. Intended for use in monitoring the environmental conditions and activity (motion) of an individual living in a senior housing community.

U.S. FDA — Device Enforcement · United States · 2013-04-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1375-2013
Date of alert
2013-04-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Intel-GE Care Innovations LLC
Product category
device
Product type
Devices
Reported risk: Customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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