Events

Recall of Power supply, battery pack

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by ResMed (Australia) 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
    21547
  • Event Initiated Date
    2017-06-19
  • 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: ResMed (NZ) Ltd, 266 Runciman Road, Pukekohe, Auckland
  • Reason
    The manufacturer has received a small number of report regarding the performance of the internal battery, where the false activation of a fuse leads to shut down of the internal battery.
  • Action
    Instructions for use to be updated

Device

Power supply, battery pack
  • Model / Serial
    Model: , Affected: All Astral External Batteries and All Astral battery packs (spares)
  • Manufacturer
    ResMed (Australia) Ltd

Manufacturer

ResMed (Australia) Ltd