Alerta De Seguridad para BioConcept RESIST-3 O.K.N. K-set

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

¿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
    2017-02-15
  • Fecha de publicación del evento
    2017-02-15
  • 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: coris bioconcept resist-3 o.K.N. k-set medical device manufacturer, coris bioconcept, has issued a field safety notice concerning its resist-3 o.K.N. k-set [product code: sun-1kr5; model (lot number): cassette (1kr5k1618); catalogue number: k-15r5; manufacturing date: 12 dec 2016; expiry date: 17 may 2017]. according to the manufacturer, there is a slight shift between the test lines oxa-48 (o) and kpc (k) of the strip and the labeled inscription on the cassette. both test lines of strip are slightly lower than the letter ‘o’ and ‘k’ labeled on the cassette. the problem has been detected by a collaborative contact during some laboratory tests. there is a potential risk of confusing the kpc line with the oxa-48 line when only the kpc signal is readable after the test. a wrong interpretation could impact the treatment received by the patient. the performance of the test is not altered at all and the affected lot meets the manufacturer’s quality standards. to facilitate interpretation of the result, it is recommended to indicate the position of the kpc green line before starting the test. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 15 february 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Coris BioConcept RESIST-3 O.K.N. K-set
  • Manufacturer

Manufacturer