Events

Recall of PROGRESSA INTEGRATED AIR SURFACE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by HILL-ROM CANADA 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
    18915
  • Event Risk Class
    III
  • Event Initiated Date
    2014-03-17
  • 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
    Hill-rom has become aware that certain progressa beds with integrated mattresses may have a potential issue during turn assist mode. an error code 31c9 may be displayed on the graphical user interface and the wrench light will turn on indicating service required. the 31c9 error means the turn assist bladder is unable to hold the required pressure to operate as intended.

Device

PROGRESSA INTEGRATED AIR SURFACE
  • Model / Serial
    Model Catalog: P7520A23 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: P7520A3 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: P7520A19 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: P7520A21 (Lot serial: >10 NUMBERS CONTACT MFG)
  • Product Description
    PROGRESSA BED MATTRESS
  • Manufacturer
    HILL-ROM CANADA LTD.

Manufacturer

HILL-ROM CANADA LTD.