Alerta De Seguridad para Atlantis PV 15 MHz Peripheral Imaging Catheter

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

¿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
    2014-01-17
  • Fecha de publicación del evento
    2014-01-17
  • 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: boston scientific atlantis pv 15 mhz peripheral imaging catheter medical device manufacturer, boston scientific, has issued a medical device safety alert concerning atlantis pv 15 mhz peripheral imaging catheter. details of affected products are as follows: material number (upn): h749364560 catalogue number: 36456 lot numbers: 16159358, 16183964, 16230195, 16230673, 16247263, 16257809, 16268498, 16289177, 16311356, 16330543, 16342824, 16419885, 16420624, 16420903, 16447744, 16458536, 16486133, 16494530 expiration date: 11 jun 2014 to 29 oct 2014 the manufacturer has become aware that the manifold of certain lots may be blocked by excess bonding adhesive. a blocked manifold may prevent affected catheter from advancing over the guidewire resulting in a delay in procedure while the device is exchanged for another unit. the manufacturer advises users to discontinue the use of and segregate the recalled product immediately. the product should be returned to the manufacturer for replacement. according to the local supplier, the affected products were not distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 17january2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Boston Scientific Atlantis PV 15 MHz Peripheral Imaging Catheter
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    DH