Events

Recall Or Safety Alert for Antibody identification panel "Data-Cyte Plus 3%", Reference 213392, lot number 612013001, manufactured by Medion Grifols Diagnostics AG, Switzerland.

According to Agencia Española de Medicamentos y Productos Sanitarios (Via FOI), this recall or safety alert involved a device in Spain that was produced by Medion Grifols Diagnostics AG.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Recall / Safety Alert
  • Date
    2013-03-01
  • Event Country
    Spain
  • Event Source
    AEMPSVFOI
  • Notes / Alerts
    The data from Spain is current through June 2018. All of the data comes from Agencia Española de Medicamentos y Productos Sanitarios, 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 Spain.
  • Extra notes in the data
  • Action
    Cell # 6 of certain references and batches of the "Data-Cyte Plus" panel manufactured by Medion Grifols Diagnostics AG, Switzerland, may have abnormal reactions depending on the Anti-D reagent used but can not be classified as Dweak cells.

Device

Antibody identification panel "Data-Cyte Plus 3%", Reference 213392, lot number 612013001, manufa...

Manufacturer

Medion Grifols Diagnostics AG
  • Manufacturer Parent Company (2017)
    Grifols Sa
  • Source
    AEMPSVFOI