Events

Recall of BD PHOENIXSPEC AP CALIBRATOR KIT

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
    93459
  • Event Risk Class
    III
  • Event Initiated Date
    2016-06-08
  • 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
    Bd has determined that the bd phoenix spec calibrator kits are labelled with incorrect expiration date.Correct date october 3o 2016. incorrect date printed october 30 2018.

Device

BD PHOENIXSPEC AP CALIBRATOR KIT
  • Model / Serial
    Model Catalog: 440911 (Lot serial: 5327782)
  • Product Description
    BD PHOENIXSPEC AP CALIBRATOR KIT
  • Manufacturer
    BECTON DICKINSON CANADA INC.

Manufacturer

BECTON DICKINSON CANADA INC.