Recall of Radiometer ABL800 series blood gas analyser with FLEXQ module

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Radiometer Medical ApS.

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
    22096
  • Event Initiated Date
    2018-01-09
  • Event Country
  • Event Source
    NZMMDSA
  • Event Source URL
  • Notes / Alerts
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • Extra notes in the data
    Recalling Organisation: Radiometer Pacific, Unit 3, 33 Spartan Road, Takanini 2105
  • Reason
    It has come to the manufacturers attention that in certain situations, the registration receipt received after placing a sampler in the flexq can be associated with a different sampler if the barcode quality on the receipt has been affected., update:, the manufacturer has now released the software upgrade version6.18 which is the corrective action for the issue reported., a checksum has been added to the barcode on the registration receipt to make the barcode more robust.
  • Action
    Software to be upgraded

Device

  • Model / Serial
    Model: , Affected: Sampler Registration receipt data, All serial numbers
  • Manufacturer

Manufacturer