Events

Safety Alert for newport ht70 and ht70 plus ventilators

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Newport Medical Instruments Inc.

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
    2012-09-14
  • Event Date Posted
    2012-09-14
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120914a.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: newport ht70 and ht70 plus ventilators the united states food and drug administration (fda) has issued a class i recall concerning newport ht70 and ht70 plus ventilators, manufactured by newport medical instruments inc. the affected products are being recalled due to a component failure on the control board which may emit a continuous high priority alarm and the ventilator may stop ventilating. for details, please refer to the following fda website: http://www.Accessdata.Fda.Gov/scripts/enforcement/ enforce_rpt-product-tabs.Cfm?action=select&recall_numbe r=z-2250-2012&w=09122012&lang=eng if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 14 september 2012.

Device

newport ht70 and ht70 plus ventilators

Manufacturer

Newport Medical Instruments Inc
  • Manufacturer Parent Company (2017)
    Medtronic plc
  • Manufacturer comment
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    DH