Events

Safety Alert for CDI H/S Cuvettes

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Terumo Cardiovascular Systems.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2016-01-13
  • Event Date Posted
    2016-01-13
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20160113.html
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: terumo cvs cdi h/s cuvettes medical device manufacturer, terumo cardiovascular systems (terumo cvs), has issued a medical device safety alert concerning its cdi h/s cuvettes. the manufacturer has received complaints of the cdi system 500 monitor displaying the "h/s disconnect at cuvette" error message when the cdi h/s cuvette does not make a proper connection to the cdi h/s probe. in this situation, blood parameter values for hct, hgb, and so2 do not display. the manufacturer has determined that this issue originated from a supplier process related to a component of the cdi h/s cuvettes, and has taken corrective action. there are no reported injuries as a result of this issue. if failure of the cdi h/s cuvette connection is recognized after initiation of cardiopulmonary bypass (cpb), the clinician will have to choose between changing out the cuvette (which requires the interruption of cpb for an indeterminate amount of time) or relying on intermittent discreet blood gas analysis values to trend hematocrit/saturation (h/sat) values (which may be contrary to hospital protocol). the manufacturer recommends affected users to take the following actions:- upon attachment of the cdi h/s cuvette to the cdi h/s probe on the cdi system 500 monitor, verify that a connection is established prior to initiating cpb. this can be confirmed visually on the cdi system 500 monitor by placing the unit in "operate" mode. if the cdi h/s cuvette does not establish connection to the cdi h/s probe (as evidenced by the “h/s disconnect at cuvette” error message on the cdi system 500 monitor display), try repositioning the cuvette in the probe head. if repositioning the cuvette in the probe head does not result in a successful connection and error-free monitor display, replace the cdi h/s cuvette using aseptic technique. if users experience an "h/s disconnect at cuvette" error message that they are not able to resolve, they should follow their complaint reporting protocol and contact the manufacturer. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 13 january 2016.

Device

CDI H/S Cuvettes

Manufacturer

Terumo Cardiovascular Systems