Events

Recall of 1235 AUTODELFIA SYSTEM - PLATE PROCESSOR - CLASS 3

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
    92071
  • Event Risk Class
    III
  • Event Initiated Date
    2013-05-27
  • 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
    Autodelfia instrument software v2.1 or higher does not fill the sample processor tubing with system liquid (wash concentrate) as designed prior to initiating an assay run. the recall is limited to autodelfia instruments that possess sample processor front-end modules (1297-014). autodelfia instruments with only plate processor modules are not affected.

Device

1235 AUTODELFIA SYSTEM - PLATE PROCESSOR - CLASS 3
  • Model / Serial
    Model Catalog: 1297-014 (Lot serial: ALL); Model Catalog: 1235-714 (Lot serial: ALL)
  • Product Description
    1235 AUTODELFIA SYSTEM - PLATE PROCESSOR - CLASS III
  • Manufacturer
    PERKINELMER HEALTH SCIENCES CANADA INC.

Manufacturer

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