Events

Alerta De Seguridad para BD Preset™ Arterial Blood Collection Syringe

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

¿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
    2012-06-07
  • Fecha de publicación del evento
    2012-06-07
  • País del evento
    Hong Kong
  • Fuente del evento
    DH
  • URL de la fuente del evento
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120607a.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:bd preset™ arterial blood collection syringe medical device manufacturer, becton, dickinson and company (bd), has issued a medical device safety alert on bd preset™ arterial blood collection syringe (catalogue number: 364314, lot number : 1174615). bd is conducting a recall on the above referenced product with the specific lot number listed, as a small percentage of syringes in the lot may be incorrectly sealed. this causes adverse impacts to the unit package integrity and product sterility since the flow wrap pouch was not sealed along its length. appropriate corrective actions have been instituted to address this condition. according to bd, the affected products have been distributed in hong kong. bd and the local distributor, united italian corp (hk) ltd., are recalling the affected products. if you are in possession of the product, please contact your supplier for necessary actions. posted on 7 june 2012.

Device

BD Preset™ Arterial Blood Collection Syringe
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: BD Preset™ Arterial Blood Collection Syringe
  • Manufacturer
    Becton

Manufacturer

Becton