Events

Recall of CHAIRMAN 2K POWERED WHEELCHAIR

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

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
    16102
  • Event Risk Class
    II
  • Event Initiated Date
    2003-09-09
  • 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
    One of the wheelchair motors needed a grounding strap to ensure that the motors are at the same voltage potential as the chassis of the wheelchair.

Device

CHAIRMAN 2K POWERED WHEELCHAIR
  • Model / Serial
    Model Catalog: (Lot serial: S/N 4100019 TO 4100225); Model Catalog: (Lot serial: S/N 1100155 TO 1102472)
  • Product Description
    CHAIRMAN 2K POWERED WHEELCHAIR
  • Manufacturer
    SOLUTION CM

Manufacturer

SOLUTION CM
  • Manufacturer Address
    JONQUIERE
  • Source
    HC