Events

Recall of Easypump LT 60-24

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 B.Braun Medical.

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
    2003-03-24
  • Event Country
    France
  • Event Source
    ANSM
  • Event Source URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/retrait-de-lots-de-diffuseur-portable-easypump-distribue-par-b-braun-medical2
  • 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
    In agreement with the Agency and at the request of the manufacturer I Flow Corporation, B.Braun Medical withdraws lot 2A2469 from reference 4434366 (code ACL 7732060) B10 and lot 2A2470 from reference 4434367 (code ACL 7403965) B1 of the medical device called portable diffuser Easypump LT 60-24 following a report for flow too fast .. Given the reduced number of recipients of the batches concerned, they were warned directly by B.Braun Medical.

Device

Easypump LT 60-24
  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
    B.Braun Medical

Manufacturer

B.Braun Medical