Recall of Oxoid Anti-microbial Susceptibility Testing Disc for Nitrofurantoin. 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 Oxoid 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-2012-RN-01246-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2012-12-10
  • 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
    A technical investigation has indicated that cartridges of the affected lots may present atypical results. continued use could result in a false indication of sensitivity to nitrofurantoin.
  • Action
    Return affected lots to Oxoid Australia for replacement with unaffected stock.

Device

  • Model / Serial
    Oxoid Anti-microbial Susceptibility Testing Disc for Nitrofurantoin. An in vitro diagnostic medical device (IVD)F200 (Nitrofurantoin)CT0035BLots 1194943 F300 (Nitrofurantoin)CT0036BLots 1191121An in vitro diagnostic medical device (IVD)
  • Manufacturer

Manufacturer