FDAJanuary 19, 2016device

CDI H/S Cuvette, non-sterile, Manufactured by Terumo Cardiovascular Group, Perfusion Pack or Smart Perfusion Pack. Product Usage: Heart/Lung Perfusion Pack is either a customized tubing pack built to user specifications or a stock tubing pack, designed for use during surgery requiring cardiopulmo...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error message when the CDI HIS Cuvette does not make a proper connection with the CDI H/S Probe. When this occurs, blood parameter values for HCT, Hgb and S02 do not display.

What to do

FDA enforcement status: Terminated

Brands named

sorin

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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