Events

Recall of VAS-CATH GUIDEWIRE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BARD ACCESS 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
    139785
  • Event Risk Class
    II
  • Event Initiated Date
    2001-03-08
  • 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
    Guidwire may have been put into the trigger guidewire dispenser backwards resulting in possibility of vein puncture.

Device

VAS-CATH GUIDEWIRE
  • Model / Serial
    Model Catalog: (Lot serial: 22GJ0480)
  • Product Description
    GUIDEWIRE
  • Manufacturer
    BARD ACCESS SYSTEMS INC.

Manufacturer

BARD ACCESS SYSTEMS INC.
  • Manufacturer Address
    SALT LAKE CITY
  • Source
    HC