Recall of Device Recall GE

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by General Electric Med Systems.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    28753
  • Event Risk Class
    Class 2
  • Event Number
    Z-0850-04
  • Event Initiated Date
    2004-03-30
  • Event Date Posted
    2004-07-20
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2006-07-24
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Screen, Intensifying, Radiographic - Product Code EAM
  • Reason
    The ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
  • Action
    Field modification instructions were issued on 3/30/04 to GE field engineers who are to correct the devices at hospitals. No letter about the correction was sent to hospitals.

Device

  • Model / Serial
    All serial numbers
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    The units were distributed nationwide in the United States and worldwide.
  • Product Description
    GE Single 20 inch TV Monitor Suspension for XT Bridge, Model 46-240485P6, Catalog Number B2056EG
  • Manufacturer

Manufacturer

  • Manufacturer Address
    General Electric Med Systems, 3000 N Grandview Blvd, Waukesha WI 53188-1615
  • Source
    USFDA