Events

Recall of UNIFINE pen insulin injector

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 Owen Mumford Ltd.

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
    2002-11-26
  • 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-d-aiguilles-8mm-et-12mm-unifine-de-la-societe-owen-mumford-ltd
  • 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
    Owen Mumford Ltd. withdraws from the market lots beginning with 00A, 00B, 00C, 00D, 00E, 00F, 00G, 00H, 00I, 00K, 00L, 00M, 01A, 01B, 01C, 01D, 01E, 01F, 01G, 01H, 01I, 01K of the medical device called "needles 8mm and 12mm UNIFINE pen insulin injector" (respectively ACL 724 739.9 and ACL 724 738.2) due to a risk of needles partially or completely blocked. In view of the small number of recipients, Owen Mumford Ltd. informed them directly.

Device

UNIFINE pen insulin injector
  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
    Owen Mumford Ltd

Manufacturer

Owen Mumford Ltd
  • Source
    LAANSM