Events

Safety Alert for SpyScope DS Access and Delivery Catheter

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Boston Scientific.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2017-12-22
  • Event Date Posted
    2017-12-22
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20171222a.html
  • Notes / Alerts
    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.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: boston scientific spyscope ds access and delivery catheter medical device manufacturer, boston scientific, has issued a medical device safety alert concerning its spyscope ds access and delivery catheter [material number (upn): m00546600; multiple batches; expiration date range: 29 aug 2019 to 21 nov 2019]. the manufacturer is initiating a voluntary removal of certain batches of spyscope ds catheters. an internal investigation found that the working channel sleeve may not be adequately bonded inside of these devices. this may result in the working channel sleeve protruding from the camera cap located at the distal tip of the catheter. according to the manufacturer, the most common injury reported has been minor tissue damage caused by the protruding working channel sleeve scraping along the duct walls during the procedure. the most serious injury that has been reported is significant bleeding resulting in medical or surgical intervention, including hospital admission and additional procedures. affected users are instructed to remove and segregate the affected products immediately. product removal is on-going. 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 22 december 2017.

Device

SpyScope DS Access and Delivery Catheter
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Boston Scientific SpyScope DS Access and Delivery Catheter
  • Manufacturer
    Boston Scientific

Manufacturer

Boston Scientific
  • Manufacturer Parent Company (2017)
    Boston Scientific
  • Manufacturer comment
    “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