Events

Safety Alert for Zoom Latitude Programmer/Recorder/Monitor

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

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
    2012-06-27
  • Event Date Posted
    2012-06-27
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120627a.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 zoom latitude programmer/recorder/monitor the health canada posted a medical device recall notice concerning zoom latitude programmer/recorder/monitor, manufactured by boston scientific corporation. the manufacturer found that some model 3120 programmers distributed in canada are mislabeled. the affected programmers do not included software to program confient implantable cardioverter defibrillator and livian cardiac resynchronization therapy-defibrillator. the software models are model 2888 and model 2945 respectively for confient and livian. model 3120 programmers with missing model 2888 and 2945 software will not be able to interrogate or program confient/livian defibrillators until the software has been loaded. according to the local supplier, the affected products were not distributed in hong kong. for details, please refer to the health canada website: http://www.Hc-sc.Gc.Ca/dhp-mps/compli-conform/recall-retrait/ _list/rec-ret_md-im_date_apr-june_2012-eng.Php if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 27 june 2012.

Device

Zoom Latitude Programmer/Recorder/Monitor
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Boston Scientific Zoom Latitude Programmer/Recorder/Monitor
  • Manufacturer
    Boston Scientific Corporation

Manufacturer

Boston Scientific Corporation
  • 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