Recall of Bard Australia Pty Ltd - Heating unit, pad, water

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

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
    22236
  • Event Initiated Date
    2017-11-09
  • 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: Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics, 54 Carbine Road, Mt Wellington, AUCKLAND
  • Reason
    The manufacturer has determined that this issue affects specific lots of arcticgel ™ pad kits. the affected units have the potential for there to be insufficient adhesion of the hydrogel to the pad. this can be easily identified if the hydrogel peels away with the release liner.
  • Action
    Manufacturer to issue advice regarding use

Device

  • Model / Serial
    Model: , Affected: ArcticGel Pad Universal Lots NGAW3898, NGBP1302, ArcticGel Cooling Kit Small Lots NGAZ2312, NGBN2492, ArcticGel Cooling Kit Medium Lot NGBN3536
  • Manufacturer

Manufacturer