Events

Recall of ACUITY

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by VARIAN MEDICAL SYSTEMS INC..

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
    27262
  • Event Risk Class
    I
  • Event Initiated Date
    2008-08-29
  • Event Country
    Canada
  • 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
    Fingers could be caught in pinch points (eg. under the couch the rail) while using or moving the exact couch. this can cause injury ranging from minor laceration to serious injury.

Device

ACUITY
  • Model / Serial
    Model Catalog: H77 (Lot serial: H770166); Model Catalog: H77 (Lot serial: H770184); Model Catalog: H72 (Lot serial: H720869); Model Catalog: H72 (Lot serial: H721036); Model Catalog: H72 (Lot serial: H720650)
  • Product Classification
    Radiology Devices
  • Product Description
    ACUITY
  • Manufacturer
    VARIAN MEDICAL SYSTEMS INC.

Manufacturer

VARIAN MEDICAL SYSTEMS INC.