Events

Recall of BV PULSERA MOBILE C-ARM SYSTEM - 9 IN. AND 12 IN. VERSIONS

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PHILIPS ELECTRONICS LTD..

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
    130873
  • Event Risk Class
    II
  • Event Initiated Date
    2008-08-15
  • Event Country
    Canada
  • 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
    Due to reliability problems with the stand-trolley cable communication between stand and trolley may not be optimal. this intermittently may result in a system not functioning properly.

Device

BV PULSERA MOBILE C-ARM SYSTEM - 9 IN. AND 12 IN. VERSIONS
  • Model / Serial
    Model Catalog: NMCA106 (Lot serial: ); Model Catalog: MMC 1951 (Lot serial: ); Model Catalog: MMC 1921 (Lot serial: )
  • Product Description
    BV PULSERA MOBILE C-ARM SYSTEM-9&12inch
  • Manufacturer
    PHILIPS ELECTRONICS LTD.

Manufacturer

PHILIPS ELECTRONICS LTD.
  • Manufacturer Address
    MARKHAM
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    HC