Events

Retiro De Equipo (Recall) de Device Recall Screw inserter (screwdriver orthopedic manual surgical instrument)

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 SpineFrontier, Inc..

¿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
    64984
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1926-2013
  • Fecha de inicio del evento
    2013-03-14
  • Fecha de publicación del evento
    2013-08-08
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2015-06-03
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=117582
  • 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
    screwdriver - Product Code HXX
  • Causa
    Inserters have a set screw that fixes a collar to the inserter. the screw set can loosen and fall out of the inserter which allows the collar to slide off the proximal end of the inserter. when the collar is not in place the locking sleeve can also slide off the inserter.
  • Acción
    Spine Frontier sent an email dated December 10, 2012, to the affected customers that a Pedfuse Inserter with part number PM3979 needed to be returned. Further questions please call (978) 232-3990.

Device

Device Recall Screw inserter (screwdriver orthopedic manual surgical instrument)
  • Modelo / Serial
    Lot Number: PM3979
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Distribution only in Texas.
  • Descripción del producto
    Rev E PedFuse Return Screw Inserter, Part Number: 11-80030 || Screw inserters are instruments which capture, hold and drive pedicle screw assemblies. There is a capturing feature that engages and holds the screw in place. There is also a feature used to lock the screw to the inserter before insertion of the screw. They can also be used to remove screws or back screws out. Screw inserters are used during the implantation of spinal pedicle screws intended to provide immobilization and stabilization of spinal segments in skeletally mature patients. Used in conjunction with Pedicle Screw Spinal system marketed as KRD1 PedFuse Pedicle Screw System .
  • Manufacturer
    SpineFrontier, Inc.

Manufacturer

SpineFrontier, Inc.
  • Dirección del fabricante
    SpineFrontier, Inc., 500 Cummings Ctr Ste 3500, Beverly MA 01915-6516
  • Empresa matriz del fabricante (2017)
    SpineFrontier, Inc.
  • Source
    USFDA