Alerta De Seguridad para Zevex Ambulatory Infusion PumpsPainsmart IOD, 6000 CMS, and 4000 CMS

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Zevex 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
    2011-11-15
  • 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.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Health canada type i recall: zevex ambulatory infusion pumpspainsmart iod, 6000 cms, and 4000 cms it has come to our attention that the health canada has issued a type i recall to remind healthcare providers and patients that painsmart iod, 6000 cms and 4000 cms (ambulatory infusion pumps), which are manufactured by zevex inc. (also traded as moog medical devices group), may give an inaccurate infusion. the accuracy of infusion with a syringe varies widely depending on the medication and stiction between the barrel and plunger of individual syringes. the effects of the variables have made the accuracy difficult to evaluate as each condition produces differing effects from the syringe variables. therefore, zevex is not confident in providing accuracy percentages for syringes as they may be misleading if the application conditions are also considered. as a result, the labeling will be modified to indicate the accuracy of delivery from a syringe cannot be guaranteed. for details, please refer to the health canada website: http://www.Hc-sc.Gc.Ca/dhp-mps/compli-conform/recall-retrait/_list/ rec-ret_md-im_date_oct-dec_2011-eng.Php if you are in possession of the affected product, please contact your supplier for necessary actions.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Zevex Ambulatory Infusion Pumps Painsmart IOD, 6000 CMS, and 4000 CMS
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH