Alerta De Seguridad para Sarns™ Sternal Saw I System

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

¿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
    2011-11-23
  • 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
    Field safety notice: terumo cvs sarns™ sternal saw i system medical device manufacturer, terumo cardiovascular system (terumo cvs), has issued an field safety notice concerning sarns™ sternal saw i system. terumo cvs has received one report of minute metal shavings leaking from the sarns™ sternal saw i system at the point where the saw blade is inserted into the saw hand piece. if metal shavings fall into the surgical site, the immediate and long range effect on the patient would be determined by the volume of metal and whether or not any other residue form inside the saw also leaked into the wound. the body would recognize the presence of the material as a foreign surface and would initiate an inflammatory response, which would range in severity from a mild localized response to a major systemic inflammatory response. either of these could lead to an increase in morbidity to the cardiac surgery patient. no patient injury and no impact to the surgical procedure were reported with this incident. terumo cvs is removing all sternal saw i system from the field. according to the manufacturer, hong kong is not affected. if you are in possession of the affected products, please contact your supplier for necessary actions. .

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Terumo CVS Sarns™ Sternal Saw I System
  • Manufacturer

Manufacturer