Events

Rappel 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

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Boston Scientific Pty Ltd.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    RC-2018-RN-00133-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2018-03-13
  • Pays de l'événement
    Australia
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2018-RN-00133-1
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
  • Cause
    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.
  • Action
    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...
  • Modèle / numéro de série
    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
  • Société-mère du fabricant (2017)
    Boston Scientific
  • Commentaire du fabricant
    “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