FDA recall record

Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas recall — FDA Z-1769-2019

An intermittent failure which causes a blender initialization fault upon start-up or during an EPGS calibration attempt leads to the Central Control…

Class IIclassification
Z-1769-2019official record ID
Jun 19, 2019report date

Recall record at a glance

Official recordZ-1769-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTerumo Cardiovascular Systems Corporation
Report dateJun 19, 2019
Recall initiation dateOct 17, 2018
Quantity72
LocationAnn Arbor, MI, United States

Official product description

Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI 00886799000588. Used in cardio-pulmonary bypass.

Why the product was recalled

An intermittent failure which causes a blender initialization fault upon start-up or during an EPGS calibration attempt leads to the Central Control Monitor control sliders being disabled, such that the gas system can only be controlled by the local control knobs.

Distribution information

Distribution US nationwide, including CA, CT, IL, IN, KY, MI, MN, MO, MT, NM, NY, OH, and WI. Foreign distribution to Canada, Mexico, and South Korea.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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