Events

Retiro De Equipo (Recall) de Ceiling Suspensions

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 Stryker Communications Corp.

¿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
    55477
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1645-2010
  • Fecha de inicio del evento
    2010-04-15
  • Fecha de publicación del evento
    2010-05-21
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-01-24
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=90975
  • 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
    Anesthesia Cabinet, Table, or Tray - Product Code BRY
  • Causa
    Installation records are incomplete.
  • Acción
    An Urgent: Medical Device Product Correction customer notification letter, dated 4/15/2010, has been sent out to all affected accounts via regular mail in the form of a certified, return request receipt letter. Accounts will receive a follow-up phone call from a Stryker Representative to schedule a re-inspection of equipment to see if it mets established critical specifications or not. The firm recommends that customers continue using all Stryker Communications products listed in the notice. Questions can be directed to Katie Blackwell at 972-410-7660 or via email at StrykerCommunicationsRA@stryker.com.

Device

Ceiling Suspensions
  • Modelo / Serial
    Product installed Between January 1, 2008 and August 31, 2009.
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Ceiling Suspensions (Surgical Light and Flat Panel Suspensions); Catalog Numbers: 0682000863, 06820001009, 0682001010, 0682001076, 0682000864, 0682000857, 0682000858, 0682001077, 0682000865, 0682001011, 0682001078, 0682000866, 0682001012, 0682001080, 0682000867, 0682000959, 0682001079, 0682000850, 0682000851, 0682000852, 0682001269, 0682001567, 0682001569, 0682001570, 06820012691, 06820015671, 06820015691, & 0680015701. || The ceiling suspensions are available in different configurations; they can hold monitors (flat panel suspensions), cameras (navigation suspensions arms) or surgical lights. The flat panel could have fixed or adjustable monitor yokes and may be single or dual arm configuration. Each ceiling suspension could hold a maximum of two surgical lights and either one camera or one monitor. There may be multiple ceiling/boom suspensions in an operating room. || Intended for use as ceiling-mounted devices for supporting or positioning surgical lights, cameras, and/or monitors.
  • Manufacturer
    Stryker Communications Corp

Manufacturer

Stryker Communications Corp
  • Dirección del fabricante
    Stryker Communications Corp, 1410 Lakeside Pkwy Ste 100, Flower Mound TX 75028-4026
  • Empresa matriz del fabricante (2017)
    Stryker
  • Source
    USFDA