Recall of ENGEN AUTOMATED SAMPLE HANDLING SYSTEM

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
    154623
  • Event Risk Class
    II
  • Event Initiated Date
    2014-04-14
  • Event Country
  • 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
    In engen systems with tcautomation (tca) software v2.6 v3.2 and v3.5 configured with bypass modules for advia centaur abbott architect vitros and/or tosoh aia systems a sample tube carrier being released in the bypass module may not be detected and therefore the next sample to be metered may not advance for processing. no error message will be posted if this occurs. the bypass module will stop processing samples indefinitley until an operator detects the issue and intervenes.

Device

  • Model / Serial
    Model Catalog: ENGEN (Lot serial: JIM340432); Model Catalog: ENGEN (Lot serial: JIM340814); Model Catalog: ENGEN (Lot serial: JIM341055); Model Catalog: ENGEN (Lot serial: JIM341130)
  • Product Description
    ENGEN AUTOMATED SAMPLE HANDLING SYSTEM
  • Manufacturer

Manufacturer