Events

Recall of BD INTEGRA SYRINGE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BECTON DICKINSON CANADA 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
    91093
  • Event Risk Class
    III
  • Event Initiated Date
    2008-12-01
  • 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
    There was a typo error on the label of the 100 unit shelf carton. the expiry date on this label reads 2013-13 when it should read 2013-03 (designating march 2013).

Device

BD INTEGRA SYRINGE
  • Model / Serial
    Model Catalog: 305298 (Lot serial: 8078251)
  • Product Description
    bd integra 1mlTB Syringe
  • Manufacturer
    BECTON DICKINSON CANADA INC.

Manufacturer

BECTON DICKINSON CANADA INC.