Events

Alerta De Seguridad para microscan synergies plus and microscan rapid/s panels

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

¿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
    2013-09-23
  • Fecha de publicación del evento
    2013-09-23
  • País del evento
    Hong Kong
  • Fuente del evento
    DH
  • URL de la fuente del evento
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20130923a.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: siemens microscan synergies plus and microscan rapid/s panels the united states food and drug administration (fda) has issued a field safety notice concerning microscan synergies plus and microscan rapid/s panels, manufactured by siemens healthcare diagnostics, inc. the affected products are identified as follows:- synergies plus negative urine combo 1- 10444745 / b1025-106 synergies plus negative combo 2 - 10444747 / b1025-108 synergies plus negative breakpoint combo 7 - 10444748 / b1025-109 synergies plus negative urine combo 2 - 10444749 / b1025-112 synergies plus negative urine combo 5 - 10483101 / b1025-115 microscan plus negative combo 3 (sold outside of us only) – 10444600 / b1016-201 microscan plus negative urine combo 4 (sold outside of us only) - 10444601 / b1016-202 microscan plus negative breakpoint combo 4 (sold outside of us only) – 10460272 / b1016-203 microscan rapid/s panels nc3.11 (sold in japan only) - 10444792 / j1025-311 microscan rapid/s panels nc3.12 (sold in japan only) – 10444793 / j1025-312 microscan rapid/s panels nc3.33 (sold in japan only) – 10444794 / j1025-333 this field safety notice has update of affected products, concerning a medical device safety alert previously issued (with links: http://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm367217.Htm; and http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm368112.Htm). according to this field safety notice, there is confirmed increase in false susceptible and false intermediate misreads for imipenem and/or meropenum on synergies plus negative and rap id/s plus negative panels read on walk away system. for details, please visit the following fda websites: http://www.Accessdata.Fda.Gov/scripts/enforcement/enforce_rpt-event-detail.Cfm?action=detail&id=66058&w=09182013&lang=eng if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 23 september 2013.

Device

microscan synergies plus and microscan rapid/s panels

Manufacturer

Siemens Healthcare Diagnostics