Recall of 5L and 10L Prolystica Ultra Concentrate Alkaline Detergent

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Device Technologies 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-2013-RN-00570-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2013-06-13
  • 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 affected prolystica ultra concentrate alkaline detergents may not have the dangerous goods label attached to illustrate that the product is hazardous.
  • Action
    Device Technologies is providing customers with the required Dangerous Goods label, and is asking customers to affix the label to the affected product.

Device

  • Model / Serial
    5L and 10L Prolystica Ultra Concentrate Alkaline Detergent5L Prolystica Ultra Concentrate Alkaline DetergentOrder code: ST-1C12T4AP10L Prolystica Ultra Concentrate Alkaline DetergentOrder code: ST-1C12T6APARTG number: 143116
  • Manufacturer

Manufacturer