Events

Recall of 5800 Series Ultra and FiberOptix Intra-Aortic Balloon Catheters

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 Arrow.

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
    2011-01-14
  • Event Country
    France
  • Event Source
    ANSM
  • Event Source URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/catheters-a-ballonnet-intra-aortique-ultra-et-fiberoptix-de-la-gamme-5800-arrow-retrait-de-lots
  • 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
    Afssaps was informed on January 10, 2011 of a recall made by the company Arrow. The affected users have received the attached mail (14/01/2011) (58 KB). This recall follows a previous informatio. , published on the Agency's website on November 03, 2010.

Device

5800 Series Ultra and FiberOptix Intra-Aortic Balloon Catheters

Manufacturer

Arrow