Recall of Stryker System 6 Aseptic Battery Kit, aseptic housing

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

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
  • Event ID
  • Event Initiated Date
  • Event Country
  • Event Source
  • 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: Stryker New Zealand Ltd, 515 Mt Wellington Highway, Mt Wellington, AUCKLAND 1060
  • Reason
    The manufacturer has identified the above lot to have insufficient bond strength at a weld joint. therefore, the quality of the weld may not be as effective as intended. this could lead to the separation of the top section of the housing from the bottom section.
  • Action
    Product to be returned to supplier


  • Model / Serial
    Model: Catalogue: 6126-120-000, Affected: Lot Numbers: 13205 (kit) & 1312, 13210, 13209 (housings)
  • Manufacturer


  • Manufacturer Parent Company (2017)
  • Source