Recall of PRECISION 500D SYSTEM - GENERATOR

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE).

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
    26585
  • Event Risk Class
    III
  • Event Initiated Date
    2013-04-30
  • Event Country
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    There is a potential for the locking nut to loosen out of the video monitor suspension yoke which could result in impact. this will not lead to an immediate fall of the suspended monitor because it will be held in place by the remaining bushing and a screw in the absence of the locking-nut.

Device

  • Model / Serial
    Model Catalog: S0910WB (Lot serial: 00000009908GQ5); Model Catalog: S0910WB (Lot serial: 00000002609GQ6); Model Catalog: S0910WB (Lot serial: 00000009899GQ6); Model Catalog: S0910WB (Lot serial: 00000004108GQ7); Model Catalog: S0910WB (Lot serial: 00000013252GP2); Model Catalog: S0910WB (Lot serial: 00000009902GQ8)
  • Product Description
    PRECISION 500D RADIOGRAPHIC & FLUOROSCOPIC SYSTEM
  • Manufacturer

Manufacturer