translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice

According to Saudi Food & Drug Authority, this translation missing: en.activerecord.attributes.event.types.recall_field_safety_notice involved a device in Saudi Arabia that was produced by Arcomed AG.

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
    Recall / Field Safety Notice
  • Event ID
    mdprc 063 06 12 000
  • Event Initiated Date
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug 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 Saudi Arabia.
  • Extra notes in the data
    Report Source: NCAR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Reason
    The ribbon cable, which connects the display pcb with the main pcb of the pumps, may show aging effects after a certain time. this aging effect reveals mainly in stiffening of the isolation of the ribbon cable where the ribbon cable is in contact with the hinge.


  • Model / Serial
    Syramed SP6000 + Volumed VP7000 Volumed ~VP7000 Premium, Volumed ~VP7000 Classic Plus Volumed ~VP7000 Lite Syramed ~SP6000 Premium Syramed ~SP6000 Classic Plus
  • Product Description
    Syringe pump; Infusion pump
  • Manufacturer