Device Recall Philips eCareManager System

  • Model / Serial
    v3.7, v3.7.1, v3.8
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution (USA) including states of MA, MO, WI, AR, AZ, PA, SD, VA, and IN.
  • Product Description
    Philips eCareManager System, Model 865325, software versions 3.7, 3.7.1 and 3.8. || Product Usage: The Philips eCareManager System software is intended for use in data collection, storage, and clinical information management with independent bedside devices and ancillary systems that are connected either directly or through networks. The eCareManager system provides patient information and surveillance of monitored patients at the point of care location and at a remote, supplementary care location through wide area networking technology and dedicated phone lines and is solely intended for use in a hospital environment. It is not intended to be used in a home environment.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Visicu, Inc., 217 E Redwood St Ste 1900, Baltimore MD 21202-3315
  • Manufacturer Parent Company (2017)
  • Source
    USFDA