Recall of ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM - MAIN UNIT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS HEALTHCARE LIMITED.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    63296
  • Event Risk Class
    II
  • Event Initiated Date
    2015-07-02
  • Event Country
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    To notify users of the acuson s family ultrasound systems of a recent finding regarding needle guides. two transducers 6c1hd and 18l6 hd demonstrate misalignment while utilizing the on-screen guidelines. the issue occurs when using the civco biopsy attachments in combination with the acuson s family on-screen guidelines. the biopsy needle may traverse outside the on-screen guidelines. this occurs on the 6c1 hd and 18l6 hd transducers.

Device

  • Model / Serial
    Model Catalog: 10041461 (Lot serial: >10 contact manufacturer); Model Catalog: 10441730 (Lot serial: >10 contact manufacturer); Model Catalog: 10441701 (Lot serial: 211263)
  • Product Description
    ACUSON S2000
  • Manufacturer

Manufacturer

  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
  • Source
    HC