Recall of Progressa Bed System with European (OIML) Version ScaleAll Progressa Beds manufactured prior to 16 May 2016 containing European (OIML) Version Scale

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Hill-Rom Pty Ltd.

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
    RC-2016-RN-00941-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2016-07-22
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Extra notes in the data
  • Reason
    Hill-rom has become aware of a potential software issue with some progressa beds equipped with the european (oiml) version scale. the issue affects how the air system utilises data from the scale to set bladder pressure points. if the software does not convert the patient weight to the air system correctly, then in some cases the pressure setting of the bladders may be higher or lower than the optimal pressure range. in some cases, patients that are already high risk may become more susceptible to pressure ulcers. this issue does not affect the accuracy or calibration of the progressa scale weighing function. the likelihood of occurrence is less than 57/100,000 units.
  • Action
    Hill-Rom will be providing an upgrade to the software of the affected units. The upgrade allows for improved scale communications with the surface and system software, and will not affect how the scale and bed are operated. In the interim, Progressa beds equipped with the European (OIML) Version Scale may continue to be used while maintaining proper patient positioning practices.

Device

  • Model / Serial
    Progressa Bed System with European (OIML) Version ScaleAll Progressa Beds manufactured prior to 16 May 2016 containing European (OIML) Version ScaleModel Number: P7500Serial Numbers: S1 12234946, S1 11791226 and O277AW0635ARTG Number: 221346
  • Manufacturer

Manufacturer