Events

Recall of JOERNS ULTRACARE MODEL 770 AC POWERED BED

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SUNRISE MEDICAL 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
    152048
  • Event Risk Class
    II
  • Event Initiated Date
    2006-07-18
  • 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
    Issue with cb6/la27 control box/actuator system used in the actuator system on its joerns ultracare model 770.Users may experience a non functioning bed.

Device

JOERNS ULTRACARE MODEL 770 AC POWERED BED
  • Model / Serial
    Model Catalog: U770 (Lot serial: ); Model Catalog: U770-GNDAL (Lot serial: ); Model Catalog: U770AL (Lot serial: )
  • Product Description
    joerns ultracare model 770 ac pwrd beds
  • Manufacturer
    SUNRISE MEDICAL CANADA INC.

Manufacturer

SUNRISE MEDICAL CANADA INC.