Events

Recall of ARCHITECT HAVAb‐IgG Reagent Kit, ARCHITECT HAVAb‐IgM Reagent Kit

According to Health Andorra, this recall involved a device in Andorra that was produced by Abbott GmbH & Co. KG.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    ARS/2018/14881
  • Date
    2018-11-02
  • Event Country
    Andorra
  • Event Source
    HA
  • Event Source URL
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=1&data1=&data2=&tipus=PRODUCTES%20DE%20DIAGN%D2STIC%20IN%20VITRO%20-%20Retirada&titol=
  • Notes / Alerts
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Extra notes in the data

Device

ARCHITECT HAVAb‐IgG Reagent Kit, ARCHITECT HAVAb‐IgM Reagent Kit
  • Model / Serial
  • Product Description
    Alert reactive architect (enlargement)
  • Manufacturer
    Abbott GmbH & Co. KG

Manufacturer

Abbott GmbH & Co. KG
  • Manufacturer Parent Company (2017)
    Abbott Laboratories
  • Manufacturer comment
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    HA