Events

Retiro De Equipo (Recall) de Device Recall NEO(R) NonLocking screws

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por In2Bones, SAS.

¿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
  • ID del evento
    77781
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-2869-2017
  • Fecha de inicio del evento
    2017-07-13
  • Estado del evento
    Completed
  • País del evento
    United States
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=157865
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Plate, fixation, bone - Product Code HRS
  • Causa
    The firm received several customer complaints reporting some perioperative breakages of ne0411 non-locking screws when inserting the screw into the radius diaphysis.
  • Acción
    In2Bones sent a Field Safety Corrective Action letter dated July 13, 2017, to all affected customers. The consignee was directed to remove the products from distribution and return it to the recalling firm. Customers with questions were instructed to contact the Quality and Regulatory Affairs team at: +33 4 72 29 26 26/ +337 61 88 44 30 or by email: qualite@in2bones.com.

Device

Device Recall NEO(R) NonLocking screws
  • Modelo / Serial
    All batch numbers
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Worldwide Diribution - US including Tennessee; Foreign - Italy, Portugal, Spain, Switzerland, UK, and France
  • Descripción del producto
    Non-Locking screws in the following lengths: || (a) NEO(R) 0.27 - 10 mm, REF W27 ST010 || (b) NEO(R) 0.27 - 12 mm, REF W27 ST012 || (c) DRP 0.27 - 12 mm, REF W27 ST012 || (d) NEO(R) 0.27 - 14 mm, REF W27 ST014 || (e) NEO(R) 0.27 - 16 mm, REF W27 ST016 || (f) NEO(R) 0.27 - 18 mm, REF W27 ST018 || (f) DRP 0.27 - 18 mm, REF W27 ST018 || The NEOVIEW(R) Plating System is intended for fixation of intra-articular and extra-articular fractures of the distal radius and reconstruction of the distal radius. It is composed of a NEOVIEW" plate in PEEK and NE0411 screws in Ti6Al4V that are available in Locking or Non-Locking versions. The NEOVIEW411 Screw Set consists of a standard set of NE0411 screws with different lengths suitable for the implantation of a NEOVIEW9 plate for an average anatomy
  • Manufacturer
    In2Bones, SAS

Manufacturer

In2Bones, SAS
  • Dirección del fabricante
    In2Bones, SAS, 28 Chemin du petit Bois, Ecully France
  • Empresa matriz del fabricante (2017)
    In2Bones SAS
  • Source
    USFDA