Recall of Invacare Action 3 Junior Push Bar Handle

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

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
    9879
  • Event Initiated Date
    2012-07-05
  • Event Country
  • Event Source
    NZMMDSA
  • Event Source URL
  • 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
    The failure of the finger bolts can lead to injuries if control of the chair is lost.
  • Action
    Product to be modified

Device

  • Model / Serial
    Model: , Affected: Sn: 050714224781 (starting 28 June 2010 to Sn 051021027909
  • Manufacturer

Manufacturer