Events

Recall of Bio-Rad D-10 Hemoglobin A Program Reorder pack

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Bio-Rad Laboratories 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
    11182
  • Event Initiated Date
    2013-01-22
  • Event Country
    New Zealand
  • Event Source
    NZMMDSA
  • Event Source URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 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: Bio-Rad Laboratories Ltd, 189 Bush Road, Rosedale, AUCKLAND 0632
  • Reason
    Medical device correction iniitiated as a result of of customer complaints investigation for anothe product regarding calibration failure and late retention times associated with elution buffers. the company examined the potential for a similar problem with the above buffer lots. bio-rad requesting customers to discard all affected product.
  • Action
    Product to be destroyed

Device

Bio-Rad D-10 Hemoglobin A Program Reorder pack

Manufacturer

Bio-Rad Laboratories Inc