Events

Field Safety Notices about OXFORD - DIPPER

According to Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), this field safety notices involved a device in Slovenia that was produced by Joerns Healthcare.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Date
    2017-07-03
  • Event Country
    Slovenia
  • Event Source
    AMPMDRS
  • Notes / Alerts
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Extra notes in the data
  • Reason
    Onset of issues such as corrosion can occur rapidly in units older than seven (7) years and may not be externally visible. joerns healthcare strongly recommends load testing for the oxford dipper is carried out at each and every six (6) monthly inspection due to the hostile environment in which it resides and operates. the humid and corrosive nature of pool-side locations can lead to product deficiencies that may otherwise remain undetected. .

Device

OXFORD - DIPPER
  • Model / Serial
    Oxford Dipper (P/No. OP10014) Oxford Dipper (P/No. OP10013)
  • Manufacturer
    Joerns Healthcare

Manufacturer

Joerns Healthcare