Events

Recall of Stratus CS / TestPak Cardiac Troponin I

According to L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), this recall involved a device in France that was produced by DADE BEHRING.

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
  • Date
    2001-07-25
  • Event Country
    France
  • Event Source
    ANSM
  • Event Source URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/rappel-de-lots-du-reactif-stratus-cs-testpak-troponine-cardiaque
  • Notes / Alerts
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • Extra notes in the data
  • Action
    DADE BEHRING withdraws from the market batches 231071002 (per 08.09.01), 231086002 (per 23.09.01), 231141002 (per 17.11.01) and 231143002 (per 19.11.01) of the reagent called Stratus CS / TestPak Cardiac Troponin I - ref. CCTNI, following a high background resulting in an increase in the results with possibility for normal samples, to exceed the threshold value (0.06ng / ml).

Device

Stratus CS / TestPak Cardiac Troponin I
  • Model / Serial
  • Product Description
    in-vitro_medical_device
  • Manufacturer
    DADE BEHRING

Manufacturer

DADE BEHRING
  • Source
    LAANSM