Intel-GE Care Innovations LLC: Medical Device Recall in 2013 - (Recall #: Z-1375-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

QuietCare. Intended for use in monitoring the environmental conditions and activity (motion) of an individual living in a senior housing community.

Product Classification:

Class II

Date Initiated: April 4, 2013

Date Posted: June 5, 2013

Recall Number: Z-1375-2013

Event ID: 65031

Reason for Recall:

Customers at 4 facilities reported receiving duplicate alerts using the QuietCare-Networked product.

Status: Terminated

Product Quantity: 1722S; 99 Out of US

Code Information:

US QuietCare: QC200403, v.02; QC200403, v.03; QC200403, v.04; QC200405 UK QuietCare: QCE200403, v.02; QCE200403, v.03

Distribution Pattern:

US and Great Britain

Voluntary or Mandated:

Voluntary: Firm initiated