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 3M Health Care Ltd.

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 119 06 13 000
  • 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: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company
  • Reason
    The subject lots of ur4 crown kits and refills contain ll3 crowns which are incorrectly labeled as ur4 crowns.


  • Model / Serial
    Product Code 902150 (Kit) • Lot Codes N484233 and N463186 Product Code 900224 (Refill) • Lot codes N466509 and N473723
  • Product Description
    Dental product, Unitek™ Primary ,Stainless Steel Crowns - Series UR4
  • Manufacturer


  • Manufacturer Parent Company (2017)
  • Manufacturers representative
    3M company
  • Source