Events

Recall of Invacare Portugal Lifters

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Invacare Portugal.

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
    20680
  • Event Initiated Date
    2016-09-28
  • 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: Invacare NZ Ltd, 4 Westfield Place, Mt Wellington, AUCKLAND
  • Reason
    In order to prevent the possibility of the d-clip becoming damaged the manufacturer has updated the product's instructions for use to communicate in more detail the correct way to assemble the d-clip and quick release pin.
  • Action
    Instructions for use to be updated

Device

Invacare Portugal Lifters
  • Model / Serial
    Model: , Affected: Birdie Lifter D-Clip and quick release pin
  • Manufacturer
    Invacare Portugal

Manufacturer

Invacare Portugal