Recall of iChemVELOCITY Automated Urine Chemistry Systems equipped with Colour/Clarity/Specific Gravity Module. An in vitro diagnostic medical device (IVD)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Beckman Coulter Australia Pty Ltd.

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
    RC-2017-RN-00477-1
  • Event Risk Class
    Class III
  • Event Initiated Date
    2017-04-20
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Extra notes in the data
  • Reason
    The ichemvelocity colour/clarity/specific gravity module (cgm) detects and reports 11 colours as opposed to the 18 listed in the ichemvelocity operator’s manual. if the ichemvelocity automated urine chemistry system is equipped with any of the affected cgm part numbers, the following urine colours will be detected and correctly reported: colourless, straw, light yellow, yellow, dark yellow, light amber, amber, dark amber, red, blue, and green. the following urine colours will not be detected or reported: orange, light brown, brown, dark brown, light red, dark red, other. there may be a discordance between the colour of the urine that is visually apparent and the colour that is reported, for the affected colours. in a worst case scenario, a discordant urine colour might prompt an additional non-invasive workup such as a repeat urinalysis or further testing. the results from the urine chemistry and microscopy will still be correctly reported.
  • Action
    Beckman Coulter is advising users that the iChemVELOCITY Operator’s Manual will be updated to reflect colours that can be detected and reported by the affected CGMs. Furthermore, if the urine colour orange, light brown, brown, dark brown, light red, dark red or other colour than those listed as ‘can be detected and reported’ is visually observed during processing, it is recommended that users: - Consider reporting the visually observed colour reading using the laboratory’s reporting system (e.g. hardcopy, LIS). - Consider using an approved back-up analyser to process and report these samples if the colours above are needed within the laboratory.

Device

  • Model / Serial
    iChemVELOCITY Automated Urine Chemistry Systems equipped with Colour/Clarity/Specific Gravity Module. An in vitro diagnostic medical device (IVD)System Reference Numbers: 800-3564, 800-7100, 800-7103, 800-7162, 800-7163, 800-7166, 800-3061Colour/Clarity/Specific Gravity Module Reference Numbers; 700-7602, 700-7611, B93997ARTG Number: 181116
  • Manufacturer

Manufacturer