Alerta De Seguridad para Absorbable Collagen Sponge

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

¿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
    2013-06-13
  • Fecha de publicación del evento
    2013-06-13
  • 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.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: integra lifesciences absorbable collagen sponge medical device manufacturer, integra lifesciences corporation, has issued a medical device safety alert concerning certain lots of the absorbable collagen sponge (acs) which is a component of the infuse bone graft kit [model no.: 7510050, 7510100, 7510200, 7510800]. the manufacturer had identified through an internal quality assurance review of processes that may have deviated from a production process during the manufacturer of specific lots of products. the products lots in question passed all product finished goods testing, are sterile, and were tested and accepted for endotoxin levels. however, due to the process deviation, they may have been released with higher level of endotoxins than permitted by the specifications for the products. higher endotoxin levels may result in a fever in the immediate postoperative period. the manufacturer is not aware of any reports of patient injuries or other adverse events in connection with these product lots. the manufacturer recommends affected healthcare professionals to monitor their patient for a fever in the immediate postoperative period according to the standard hospital or clinician protocol. the manufacturer also advises all affected users to discontinue use of the captioned products. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 13 jun 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Integra LifeSciences Absorbable Collagen Sponge
  • Manufacturer

Manufacturer