Recall of URETHROSPIRAL 3

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 Coloplast.

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
    2009-10-21
  • 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
    On 20/10/2009, the company COLOPLAST removed from the market lot 9033484 of the reference AE1562 of the medical device called URETHROSPIRAL 3, manufactured by COLOPLAST, following the detection of an assembly anomaly that could interfere with the laying of this prosthesis. The company COLOPLAST has directly notified the recipients of the offending lot with the attached message validated (21/10/2009) (53 KB) by Afssaps. This information is addressed to the directors and correspondents of materiovigilance for diffusion if necessary to the services concerned. The relevant European Competent Authorities are informed of this measure by the manufacturer.

Device

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer

Manufacturer