Events

Retiro De Equipo (Recall) de Capio Suture Capturing Devices (SLIM, Standard, Open Access, RP) For use with:- Uphold Vaginal Support System (ARTG:150342) - Discontinued - Uphold LITE with Capi SLIM Vaginal Support System (ARTG:150342) - Discontinued - Pinnacle Anterior Pelvic Floor Repair Kit (ARTG:150342) - Discontinued- Pinnacle Posterior Pelvic Floor Repair Kit (ARTG:150342) - Discontinued - Pinnacle LITE Posterior with Capio SLIM Pelvic Floor Repair Kit (ARTG: 246992) - Discontinued

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Boston Scientific Pty Ltd.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    RC-2018-RN-00133-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2018-03-13
  • País del evento
    Australia
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2018-RN-00133-1
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    Boston scientific (bsc) have observed a gradual increasing trend in reports regarding capio suture breakage and/or detachment of the capio suture darts from both the capio suture and the pelvic floor kit mesh assembly. the mesh assembly refers to the portion of the pelvic floor delivery system which is removed from the patient following implantation of the mesh.
  • Acción
    Boston Scientific is advising customers to refer to the updated Instructions for Use detailed in the Customer Letter.

Device

Capio Suture Capturing Devices (SLIM, Standard, Open Access, RP) For use with:- Uphold Vaginal S...
  • Modelo / Serial
    Capio Suture Capturing Devices (SLIM, Standard, Open Access, RP) For use with:- Uphold Vaginal Support System (ARTG:150342) - Discontinued - Uphold LITE with Capi SLIM Vaginal Support System (ARTG:150342) - Discontinued - Pinnacle Anterior Pelvic Floor Repair Kit (ARTG:150342) - Discontinued- Pinnacle Posterior Pelvic Floor Repair Kit (ARTG:150342) - Discontinued - Pinnacle LITE Posterior with Capio SLIM Pelvic Floor Repair Kit (ARTG: 246992) - DiscontinuedARTG Number: 137473
  • Manufacturer
    Boston Scientific Pty Ltd

Manufacturer

Boston Scientific Pty Ltd
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • 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
    DHTGA