Events

Recall of EASY GO ASPIRATOR

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

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
    88898
  • Event Risk Class
    III
  • Event Initiated Date
    2004-11-23
  • 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 charger may cause an overheat problem of the easy go vac when left plugged in to an ac outlet and connected to the unit for an extended period of time.

Device

EASY GO ASPIRATOR
  • Model / Serial
    Model Catalog: (Lot serial: S/N: 008360 TO 014360)
  • Product Description
    EASY GO ASPIRATOR (UL1431) (UL2601)
  • Manufacturer
    PRECISION MEDICAL INC.

Manufacturer

PRECISION MEDICAL INC.