Retiro De Equipo (Recall) de Device Recall Fisher and Paykel Healthcare CosyCot and Kit Replacement Head

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 Fisher & Paykel Healthcare, Ltd..

¿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
    69668
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0210-2015
  • Fecha de inicio del evento
    2014-11-06
  • Fecha de publicación del evento
    2014-11-13
  • Estado del evento
    Terminated
  • País del evento
  • Fecha de finalización del evento
    2015-04-27
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
  • 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
    Warmer, infant radiant - Product Code FMT
  • Causa
    Breakage of the nut that secures the heater head in place, which can cause the heater head to become partially detached and swing towards the bassinet. there is the potential that a heater head could contact a patient situated on the bassinet and cause a serious injury.
  • Acción
    Fisher & Paykel Healthcare sent an Urgent Medical Device Recall letter to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to: Step 1: Identify any affected Infant Warmers in your inventory by checking the REF and SERIAL number on the device label (see examples in Figures 1 and 2). Step 2: Identify any affected spare parts in your inventory by checking the REF and LOT number on the parts (see example in Figure 3). Step 3: Check your Infant Warmer service records to determine if affected spare parts were installed on any other Infant Warmers. If you are unable to identify specific Infant Warmers that may have had affected spare parts installed, then please contact FPH at the contact details below. Step 4: Replacement of Affected Nut. - Remove the affected Infant Warmer from use. - Switch the warmer off and disconnect it from the mains power supply. - Support the heater head during disassembly to prevent it from falling. - Follow Steps A to F in Figure 4 below to replace the nut. - Ensure the pivot washer remains in place when installing the new nut. - Ensure that the heater head is secure, can rotate smoothly, and the detent locates the head in the central position. - Reconnect the mains power supply, switch the warmer on, and ensure there are no error codes or alarms before returning to use. Step 5: Complete the Urgent Medical Device Recall Response Form and return it to your FPH Representative

Device

  • Modelo / Serial
    Affected Serial (SN) and Lot (LOT) Numbers Infant Warmers: 071116ZZZZZZ - 090810ZZZZZZ  Spare Parts: 071116 - 090810
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) and Internationally to Albania, Algeria, Australia, Austria, Bahrain, Bangladesh, Bekgium, Bermuda, Chile, China, Croatia, Dominican Republic, Estonia, Finland, France, Germany, Great Britain, Greece, Hong Kong, Iceland, India, Indonesia, Iran, Ireland, Israel, Jordan, Kenya, Kuwait, Latvia, Lebanon, Lithuania, Malaysia, Mauritius, Mexico. Morocco, New Zealand, Nigeria, Northern Ireland, Norway, Pakistan, Palestinian Territory, Panama, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, singapore, Slovenia, South Africa, Spain, Sri Lanka, Sultanate of Oman, Syria, Taiwan, Thailand, The Netherlands, Tunisia, Turkey, United Arab Emirates, Uruguay, Venezuela, Vietnam, and West Bank.
  • Descripción del producto
    Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer || Fisher and Paykel; Healthcare CosyCot and Kit Replacement Head Case Assembly || It is designed to assist with the thermoregulation of infants weighing up to 10kg and is used by labor and delivery rooms and pediatric intensive care units. || Infant Warmers Model Number (REF) || IW910XXX, IW920XXX, IW931XXX, IW932XXX, IW933XXX, IW934XXX, IW951XXX, IW952XXX, IW953XXX, IW954XXX, IW980XXX, IW990XXX || Spare Parts Model Number (REF) || 043041129, 043041130, 043041131, 043042359, 648040142
  • Manufacturer

Manufacturer

  • Dirección del fabricante
    Fisher & Paykel Healthcare, Ltd., 15 Maurice Paykel Place, East Tamaki, Auckland New Zealand
  • Source
    USFDA