Events

Recall of Pennine Healthcare Ryles - Feeding Tubes

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Pennine Healthcare 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
    20587
  • Event Initiated Date
    2016-09-16
  • 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: Jackson Allison Medical and Surgical Ltd, 56 Lunn Ave, Mt Wellington, Auckland
  • Reason
    Possibility that a tube could have the printed graduations running the wrong way.
  • Action
    Product to be returned to supplier

Device

Pennine Healthcare Ryles - Feeding Tubes
  • Model / Serial
    Model: RT-2006 RT-2006/L RT-2008 RT-2008/L RT-2010 RT-2010/L RT-2012 RT-2012/L RT-2014 RT-2014/L RT-2016 RT-2016/L RT-2018 RT-2018/L RT-2020 RT-2108 RT-2110 RT-2112 RT-2114 RT-2116 RT-2118 RT-2306 RT-2308 RT-2310 RT-2312 RT-2314 RT-2316 RT-2318 and RT-2320, Affected: All lots
  • Manufacturer
    Pennine Healthcare Ltd

Manufacturer

Pennine Healthcare Ltd