Events

Recall of SPECIMEN GATE LABORATORY

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PERKINELMER HEALTH SCIENCES 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
    83184
  • Event Risk Class
    III
  • Event Initiated Date
    2017-07-14
  • 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 deployed specimen gate laboratory software is not functioning consistent with the configured parameters defined by the customer. the issue may result in reporting incorrect results.

Device

SPECIMEN GATE LABORATORY

Manufacturer

PERKINELMER HEALTH SCIENCES CANADA INC.
  • Manufacturer Address
    WOODBRIDGE
  • Manufacturer Parent Company (2017)
    Perkin Elmer Inc.
  • Source
    HC