Device recall

Z-0877-2013: QuietCare-Networked product, Facility Server/model: QC101601; The QuietCare…

FDA device recall · Class II · Intel-GE Care Innovations LLC

Key facts

Recall number (Z-number) Z-0877-2013
Recall event 63957
Product QuietCare-Networked product, Facility Server/model: QC101601; The QuietCare system is intended to detect and analyze residents' movements.
Product code KMI
Recalling firm Intel-GE Care Innovations LLC
Recall class Class II
Status Terminated
Termination date Feb 26, 2013
FEI number 3008850109

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)