Alerta De Seguridad para Junctional Tourniquet

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

¿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
    2014-10-09
  • Fecha de publicación del evento
    2014-10-09
  • 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: sam medical products junctional tourniquet the united states food and drug administration (fda) posted a medical device safety alert concerning the accessory (axilla) strap for the sam junctional tourniquet (sjt), manufactured by sam medical products. according to the fda, the manufacturer notified affected users of a voluntary recall to address a potential issue with a clip used to secure the accessory strap used for the axilla application of the sjt. if this piece were to fail in actual use the operator may face a potential delay in using the sjt in the axilla area. all other indications of the sjt (inguinal hemorrhage and pelvic fracture) are not impacted by this issue. the manufacturer is replacing the current axilla straps with an updated version. the manufacturer has not received any reports of patient injuries to date related to this issue nor has it been reported to fail during actual patient use. for details, please refer to the following fda websites: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm417985.Htm http://www.Fda.Gov/safety/recalls/ucm417940.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 09 october 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: SAM Medical Products Junctional Tourniquet
  • Manufacturer

Manufacturer