Events

Safety Alert for Latitude Programmer Model 3300

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
    2018-09-13
  • Event Date Posted
    2018-09-13
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20180913.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 latitude programmer model 3300 medical device manufacturer, boston scientific, has issued a medical device safety alert concerning its latitude programmer [model: 3300; description: prgmr latitude us 3300]. upon limited market release to the us in may 2018, customer complaints were received regarding the 3300 programmer integrated pacing system analyzer (psa) when attempting to evaluate lead impedances. complaints described that while pacing the ra lead, capture and pacing were also observed in the rv lead. according to the manufacturer, the pir team concludes that while the product is manufactured per specifications, the current cross chamber stimulation behaviour does not meet the intent of system requirements. therefore, the psa application reflects an increase risk to patients and a field removal is recommended to return 3300 programmers to the manufacturer. the 3300 is also in limited market release in europe. no other geographies are currently approved for the 3300-programmer use. according to the local supplier, the affected products are not distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 13 september 2018.

Device

Latitude Programmer Model 3300
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Boston Scientific Latitude Programmer Model 3300
  • 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