Alerta De Seguridad para IRISpec CA/CB/CC and IRISpec CA/CB

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

¿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
    2016-04-18
  • Fecha de publicación del evento
    2016-04-18
  • 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: iris international irispec ca/cb/cc and irispec ca/cb medical device manufacturer, iris international, has issued a medical device safety alert concerning its irispec ca/cb/cc and irispec ca/cb. the affected products are identified as follows:- reference number: 800-7211 lot numbers: 336-15, 343-15 (exp april 2016) lot numbers: 004-16,006-16,019-16,021-16,182-15 (exp may 2016) reference number: 800-7702 lot numbers: 313-15, 336-15 (exp april 2016) lot numbers: 004-16 (exp may 2016) reference number: 800-0074 lot number: 309-15 (exp april 2016) the manufacturer has become aware of an issue in which premature degradation of bilirubin for specific lots may lead to bilirubin control failures for the irispec ca bilirubin control material. the control may fail for the bilirubin analyte and laboratories will be unable to process patient samples until qc passes. there is no impact to patient results. the manufacturer is advising users to ensure the directions for handling and storage of the control material as per the instructions for use are followed to prevent premature degradation of the control material. users are advised to discard the bottle if the irispec ca control for bilirubin fails and use alternative bottles in the kit. if the problem persists, users are advised to request a product replacement from the manufacturer. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 18 april 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Iris International IRISpec CA/CB/CC and IRISpec CA/CB
  • Manufacturer

Manufacturer