Events

Recall of HF Cables

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Olympus Winter & Ibe GmbH.

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
    20643
  • Event Initiated Date
    2016-09-15
  • 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: Olympus (NZ) Ltd, 15D Paul Matthews Road, Albany, Auckland
  • Reason
    Although procedures may continue by troubleshooting and clearing error codes in accordance with the esg-400 instructions for use (ifu section 8.2), olympus would like to request your support in highlighting instances of the following error codes when the device is connected:, " e618 'data transfer',, " e486 'no instrument connected'; or,, " a pop up message 'use default instrument settings'.
  • Action
    Manufacturer to issue advice regarding use

Device

HF Cables

Manufacturer

Olympus Winter & Ibe GmbH