Events

Retiro De Equipo (Recall) de Device Recall Surgical Headlight

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 Kerr Corporation.

¿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
    63512
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0402-2013
  • Fecha de inicio del evento
    2011-11-17
  • Fecha de publicación del evento
    2012-11-20
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2012-11-20
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=114097
  • 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
    Light, surgical headlight - Product Code EBA
  • Causa
    The firm recalled the freedom cordless led headlight because some units were assembled with an incorrect component in the control board electronics that may cause some freedom cordless led headlight units to become warm to the touch; however, no skin damage will occur.
  • Acción
    Orascoptic sent an "URGENT: MEDICAL DEVICE RECALL" letter dated November 17, 2011. The letter identified the product, problem, and actions to be taken by the customers. An Acknowledgement Form was included for customers to complete and return to the firm. Contact Orascoptic Customer Care at 608-831-2555 for assistance regarding this notice.

Device

Device Recall Surgical Headlight
  • Modelo / Serial
    Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-77003470 and Freedom System, Long Length, Part Number 910863-2, Serial Numbers 77001000-77003470.   Freedom Cordless LED Light System has no expiration date. The affected units were produced and distributed since February 2011.
  • Clasificación del producto
    Dental Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-USA (nationwide) and the countries of Canada, Australia, and Europe.
  • Descripción del producto
    Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-77003470 and Freedom System, Long Length, Part Number 910863-2, Serial Numbers 77001000-77003470. || Freedom Cordless LED Light System is a Class I Medical Device. The device || listing number this product is E115952. || The intended use of this device is to illuminate oral structures and operating areas.
  • Manufacturer
    Kerr Corporation

Manufacturer

Kerr Corporation
  • Dirección del fabricante
    Kerr Corporation, 3225 Deming Way, Middleton WI 53562
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Source
    USFDA