Events

Recall of JOERNS ULTRACARE XT BED

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by JOERNS HEALTHCARE CANADA 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
    19705
  • Event Risk Class
    II
  • Event Initiated Date
    2018-01-15
  • 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
    Joerns healthcare has identified an issue with the incorrect bed model (easycare) etl/intertek label being applied to ultracare xt beds. the impacted beds were manufactured on september 8 2017.

Device

JOERNS ULTRACARE XT BED
  • Model / Serial
    Model Catalog: UCXT (Lot serial: s/n: 1000045990); Model Catalog: UCXT (Lot serial: s/n: 1000045972); Model Catalog: UCXT (Lot serial: s/n: 1000045985); Model Catalog: UCXT (Lot serial: s/n: 1000045986); Model Catalog: UCXT (Lot serial: s/n: 1000045987); Model Catalog: UCXT (Lot serial: s/n: 1000045988)
  • Product Description
    JOERNS ULTRACARE XT BED
  • Manufacturer
    JOERNS HEALTHCARE CANADA INC.

Manufacturer

JOERNS HEALTHCARE CANADA INC.