Events

Alerta De Seguridad para curlin intravenous administration sets

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

¿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
    2012-05-24
  • Fecha de publicación del evento
    2012-05-24
  • País del evento
    Hong Kong
  • Fuente del evento
    DH
  • URL de la fuente del evento
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120524.html
  • 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
    Medical device safety alert: moog curlin intravenous administration sets the united states food and drug administrations (fda) has issued a firm press release concerning the voluntary recall of selected curlin intravenous administration sets, sold and distributed in the united states between december 2011 and may 2012 and manufactured by moog medical devices group. the manufacturer found that use of the affected sets may cause desanguination (blood loss), an under-delivery of prescribed medication/fluid, or a potential delay in therapy. customer complaints have identified three out of 544,900 suspect sets manufactured for the united states. so far, the manufacturer has not received any reports injury or death as a result of this issue. for details, please refer to fda website http://www.Fda.Gov/safety/recalls/ucm305208.Htm if you are in possession of the product, please contact your supplier for necessary actions. posted on 24 may 2012.

Device

curlin intravenous administration sets
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Moog Curlin Intravenous Administration Sets
  • Manufacturer
    Moog Medical Devices Group

Manufacturer

Moog Medical Devices Group
  • Empresa matriz del fabricante (2017)
    Moog Inc
  • Source
    DH