Events

Retiro De Equipo (Recall) de Device Recall Del Medical DCTM Ceiling Tube Mount

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 Del Medical Systems Group.

¿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
    28372
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0712-04
  • Fecha de inicio del evento
    2004-02-13
  • Fecha de publicación del evento
    2004-07-20
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-09-30
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=31680
  • 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
    Tube Mount, X-Ray, Diagnostic - Product Code IYB
  • Causa
    There is a potentially defective worm gear in the tension adjusting mechanism of the balancer used in the digital ceiling mounted tube support system for overhead x-ray units.
  • Acción
    Del Medical sent a Field Correction Recall letter dated 2/13/04 to all dealers/assemblers receiving DCTM''s during the affected time frame, alerting them to potential defective worm gear. The accounts were asked to locate the systems listed in the attachment to the letter, and alert the end users to take the units out of service until they can be inspected. Follow-up letters were sent via registerd mail on 2/19/04, reiterating the 2/13/04 letter and providing the accounts with instructions for inspection of the balancers. If the worm gear fails the test, the dealers were instructed to contact Del Medical for replacement of the balancer and assure that the unit is not placed back in service until the balancer has been replaced.

Device

Device Recall Del Medical DCTM Ceiling Tube Mount
  • Modelo / Serial
    Model DCTM, serial numbers 00182-0303, 00337-0303, 00901-0503, 00948-0503, 02082-0703, 02083-0703, 02152-0703, 02153-0703, 02187-0703, 02188-0703, 02289-0703, 02460-0803, 02492-0803, 02493-0803, 02581-0803, 02730-0803, 02805-0803, 02809-0903, 02810-0903, 02811-0903, 02812-0903, 02866-0903, 02918-0903, 02989-0903, 02990-0903, 02991-0903, 03147-0903, 03148-0903, 03149-0903, 03457-1003, 03458-1003, 03544-1003, 03545-1003, 03624-1003, 03625-1003, 03756-1003, 03757-1003, 03888-1103, 03956-1103, 04085-1103, 04122-1103, 04154-1103, 04236-1103, 04248-1103, 04264-1103, 04371-1203, 04433-1203, 04439-1203, 04480-1203, 04529-1203, 04572-1203, 04634-1203, 04659-1203, 04709-1203, 00032-0104, 00085-0104, WG0031-0102-R
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nevada, Ohio, Tennessee, Nebraska, Arizona, Maryland, Wisconsin, Florida, Texas, Kansas, Oklahoma, Illinois, Colorado, California, Minnesota, Michigan, Alabama, Rhode Island and internationally to Canada, Panama and Pakistan
  • Descripción del producto
    DCTM Digital Ceiling Tube Mount, model DCTM; a fully counter-balanced radiographic x-ray tube suspension system designed to facilitate a wide range of procedures; Manufactured by Del Medical Imaging Corporation, Franklin Park, IL 60131 U.S.A.
  • Manufacturer
    Del Medical Systems Group

Manufacturer

Del Medical Systems Group
  • Dirección del fabricante
    Del Medical Systems Group, 11550 West King Street, Franklin Park IL 60131-1330
  • Source
    USFDA