Events

Recall of Aaxis Alcohol Swab

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Nantong Strip Medical Supply Co 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
    13064
  • Event Initiated Date
    2012-09-10
  • 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: TOLLOT Pty T/a Aaxis Pacific, C/O Anthony Evans CAUGHLEY,Level 1, 24 Manukau Road, Epsom, Auckland
  • Reason
    Product is labelled as containing 70% isopropanol alcohol, but has been tested and contains ethanol.
  • Action
    Product to be returned to supplier

Device

Aaxis Alcohol Swab

Manufacturer

Nantong Strip Medical Supply Co Ltd
  • Source
    NZMMDSA