Safety Alert for Carto® 3 Systems

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

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
    2012-02-21
  • Event Country
  • Event Source
    DH
  • Event Source URL
  • 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
    Field safety notice: biosense webster carto® 3 systems the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning cartor 3 systems manufactured by biosense webster, inc. the manufacturer has recently become aware that some carto® 3 systems may be susceptible to ablation radio frequency interference through certain interconnected cable configurations. according to the manufacturer, the root cause has been determined to be a newly introduced patient interface unit (piu) backplane card. the new card is more sensitive to radio frequency interference, which will manifest as a jumping/ disappearing icon and/or error messages 105 and 319. biosense webster explained that while ablation at an unintended location could potentially happen as the result of undetected or ignored icon jumps, the likelihood of this happening is remote as the high detectability of icon jumps and the verification of catheter tip position with fluoro and/or ecg by operating physicians. as a result, the probability of a potential patient injury from icon jumps is unlikely and continued use of the carto® 3 systems remains safe and effective. biosense webster is going to replace the piu backplane card for the affected customers. meanwhile, customers are suggested to eliminate the radio frequency interference by utilizing the accessories provided with the customer notification. the notification also suggests ways to deal with the error messages. for details, please refer to the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/index.Htm if you are in possession of the affected product, please contact your supplier for necessary actions.

Device

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Biosense Webster Carto® 3 Systems
  • Manufacturer

Manufacturer