Events

Retiro De Equipo (Recall) de Device Vacuum Safety Direct SV 33

Según L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en France que fue producido por AGA MEDICAL.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • Fecha
    2007-03-02
  • País del evento
    France
  • Fuente del evento
    ANSM
  • URL de la fuente del evento
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/rappel-de-lots-de-dispositif-securite-de-vide-direct-sv-33-aga-medical
  • Notas / Alertas
    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.
  • Notas adicionales en la data
  • Acción
    On 28/02/07, AGA MEDICAL proceeded with the recall of lots 2060114 (manufactured on 06/01/06), 2060472 (manufactured on 27/01/06), 2060473 (manufactured on 27/01/06), 2061261 (manufactured on March 14, 2006), 2064111 (manufactured on September 25, 2006) of the medical device called "Direct Vacuum Safety Device SV 33, P / N R311044", due to a risk of blockage of the vacuum system. suction by the safety ball component of the anti-overflow system. The company has directly notified the recipients of the incriminated lots with the message attached (28/02/2007) (52 KB) validated by Afssaps. This information is addressed to the directors of health establishments and local correspondents of materiovigilance for dissemination where appropriate to the services concerned.

Device

Device Vacuum Safety Direct SV 33
  • Modelo / Serial
  • Descripción del producto
    medical_device
  • Manufacturer
    AGA MEDICAL

Manufacturer

AGA MEDICAL
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    LAANSM