Events

Recall of NETLINK TRAVELER AMPLIFIER AMBULATORY/EEG LAB 32 CHANNEL

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BIO-LOGIC SYSTEMS CORP..

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
    23923
  • Event Risk Class
    II
  • Event Initiated Date
    2007-03-21
  • 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
    The battery pack for the ceegraph netlink traveler may be damaged and overheat if placed into the unit incorrectly.

Device

NETLINK TRAVELER AMPLIFIER AMBULATORY/EEG LAB 32 CHANNEL
  • Model / Serial
    Model Catalog: (Lot serial: 06I01203); Model Catalog: (Lot serial: 06I01027)
  • Product Description
    CEEGRAPH NETLINK TRAVELER
  • Manufacturer
    BIO-LOGIC SYSTEMS CORP.

Manufacturer

BIO-LOGIC SYSTEMS CORP.
  • Manufacturer Address
    MUNDELEIN
  • Source
    HC