Recall of KODAK DIRECTVIEW DR 7500 SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CARESTREAM HEALTH CANADA COMPANY.

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
    29708
  • Event Risk Class
    II
  • Event Initiated Date
    2014-07-10
  • 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
    Carestream has identified an issue at a customer site related to the dr 7500 beta assembly (x-ray tube and collimator) detaching from the overhead tube crane (otc) telescope. it has been determined that as a result of an impromperly assembled part which holds the beta assembly to the otc telescope an inspection of the part is needed and in addition a repair of the assembly may be required.

Device

  • Model / Serial
    Model Catalog: 879 1345 (Lot serial: 75000216); Model Catalog: 879 1345 (Lot serial: 75000233); Model Catalog: 879 1345 (Lot serial: 75000673); Model Catalog: 879 1345 (Lot serial: 75000648); Model Catalog: 879 1345 (Lot serial: 75000590); Model Catalog: 879 1345 (Lot serial: 75000150)
  • Product Description
    KODAK DIRECTVIEW DR 7500 SYSTEM
  • Manufacturer

Manufacturer

  • Manufacturer Address
    VAUGHAN
  • Manufacturer Parent Company (2017)
  • Source
    HC