Events

Field Safety Notices about MINICAP PROTEIN(E) 6

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 sebia.

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
    2017-08-24
  • 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
    Users have warned us that some buffer kits do not have the buffer they should be: 12126/01 series instead of 05096/01. our investigation showed that a human error occurred in the packaging of these kits. this mistake does not affect the quality or usefulness of the kits.

Device

MINICAP PROTEIN(E) 6
  • Model / Serial
    5096102
  • Manufacturer
    sebia

Manufacturer

sebia
  • Manufacturer Parent Company (2017)
    Sam Topco
  • Source
    AMPMDRS