Events

Recall of DIMENSION CA CALCIUM (CA-F)

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DADE BEHRING 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
    15412
  • Event Risk Class
    III
  • Event Initiated Date
    1998-10-02
  • 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
    Inconsisitent well to well test results which contains a discoloured reagent which can cause inaccuracies of 0.7 mg/dl at 8 mg/dl level and 1.3 md/dl at the 14 mg/dl level.

Device

DIMENSION CA CALCIUM (CA-F)
  • Model / Serial
    Model Catalog: DF23 (Lot serial: JP7288)
  • Product Description
    DIMENSION CA CALCIUM (CA-F)
  • Manufacturer
    DADE BEHRING CANADA INC.

Manufacturer

DADE BEHRING CANADA INC.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC