Alerta De Seguridad para Merit 7F Prelude Short Sheath Introducers

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

¿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
    2017-03-31
  • Fecha de publicación del evento
    2017-03-31
  • 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: merit 7f prelude short sheath introducers the united states food and drug administration (fda) has issued a medical device safety alert concerning merit 7f prelude short sheath introducers [lot numbers: h1041469, h1041473, h1036880, h1041464; catalogue numbers: k15-00070, k15-00170, pss-7f-4-035mt, pss-7f-4mt; manufacturing dates: 23 nov 2016 to 30 nov 2016; distribution dates: 15 dec 2016 to 18 jan 2017], manufactured by merit medical systems, inc. the manufacturer is recalling the prelude short sheath introducer due to a manufacturing defect which may cause the tip to separate from the sheath during the insertion procedure. if this occurs, the tip could enter the patient's bloodstream. this may result in prolonged procedure times, additional surgery to remove the tip from the patient, blood clots, internal tears and perforation to arteries or veins, excessive bleeding, and death. the manufacturer advises users to quarantine and discontinue use of the affected products and return them to the manufacturer. for details, please refer to the fda website: https://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm549795.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 31 march 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Merit 7F Prelude Short Sheath Introducers
  • Manufacturer

Manufacturer