Alerta De Seguridad para PLUM LifeCare 5000 Series and PLUM XL Families of Infusers

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Hospira Inc.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2013-12-12
  • Fecha de publicación del evento
    2013-12-13
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: hospiraplum lifecare 5000 series and plum xl families of infusers the australia therapeutic goods administration (tga) posted a medical device safety alert concerning plum lifecare 5000 series and plum xl families of infusers manufactured by hospira inc.The affected products are identified as follows:- plum lifecare 5000, list number: 02507 plum xl, list number :11555 plum xlm, list number: 11846 plum xld, list number: 11859 the door roller assembly on the plum a lifecare 5000 series and plum xl has the potential to break which can lead to possible unrestricted flow and/or over delivery during the removal of the iv administration set's cassette from the pump. the manufacturer is requesting hospitals to take the following steps to inspect the door assemble prior to loading the cassette: open the cassette door by pulling on the lever; unlatch the cassette door by pushing on the door release tab and pulling the door down; visually inspect the door roller pin for any evidence of the damage or door roller misalignment; and ensure that the door roller spins smoothly with a finger touch. if any door rollers or pins appear loose, broken or missing, hospira advises users to remove the device from use. the manufacturer is in the process of retiring the plum lifecare 5000 and plum xl in 2015. for details, please visit the following tga website:http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-01288-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 13 december 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: HospiraPLUM LifeCare 5000 Series and PLUM XL Families of Infusers
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH