Events

Recall of ID MICRO TYPING SYSTEM - SICKLE CELL TEST

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by ORTHO-CLINICAL DIAGNOSTICS.

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
    79810
  • Event Risk Class
    II
  • Event Initiated Date
    2005-04-25
  • 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
    The manufacturer has received reports of decreased reactivity in some vials and there is a risk of false negative results.

Device

ID MICRO TYPING SYSTEM - SICKLE CELL TEST
  • Model / Serial
    Model Catalog: 04170 040012 (Lot serial: 04170.21.11)
  • Product Description
    DIAMED AG ID-HBS REDUCING AGENT
  • Manufacturer
    ORTHO-CLINICAL DIAGNOSTICS

Manufacturer

ORTHO-CLINICAL DIAGNOSTICS