Events

Recall of Howard Wright M9 Bed Range

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Howard Wright 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
    15344
  • Event Initiated Date
    2013-09-17
  • 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: Howard Wright Ltd, Paraite Road, Bell Block, New Plymouth
  • Reason
    Potential for the side rails to unlatch at a force less than specified in as/nzs3200.2.38:2007.
  • Action
    Product to be modified

Device

Howard Wright M9 Bed Range
  • Model / Serial
    Model: M9 Ward, M9 Compact beds, Affected: Manufactured between Nov-2011 and Jun-2013
  • Manufacturer
    Howard Wright Ltd

Manufacturer

Howard Wright Ltd