Recall of Ambulance Pumps Cassettes Cadd

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 SMITHS 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
    2008-01-18
  • Event Country
  • Event Source
    ANSM
  • Event Source URL
  • 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 Afssaps, the company Smiths Medical, informed January 15, 2008, the users of cassette cassettes for pumps Cadd outpatient recall of some batches .. This recall is made because of a risk of leakage of these tapes, which had already been the subject of a mail in June 2007. The users concerned, in France, received the attached mail (15/01/2008) (22 ko) .. This information is address to providers, directors of health establishments and local correspondents of materiovigilance for dissemination to the services concerned. Information of the 03/07/200. concerning infusion pump cassettes Cad. Information from 01/10/200. on Updating Information on Cadd Ambulatory Infusion Pumps

Device

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer

Manufacturer

  • Source
    LAANSM