Events

Recall of DISINFECTION SYSTEM - 208 VOLTAGE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by JOHNSON & JOHNSON MEDICAL PRODUCTS A DIV. OF JOHNSON & JOHNSON 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
    154410
  • Event Risk Class
    III
  • Event Initiated Date
    2013-04-01
  • 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
    Advanced sterilization products has determined that under certain circumstances the evotech endoscope cleaner and reprocessor system may not properly calculate the expiration date of the cidezyme xtra multi enzymatic detergent from the information entered by the user. in these circumstances the expiration date displayed on the evotech ecr screen is one month after the labeled expiration date.

Device

DISINFECTION SYSTEM - 208 VOLTAGE

Manufacturer

JOHNSON & JOHNSON MEDICAL PRODUCTS A DIV. OF JOHNSON & JOHNSON INC.