FDA recall record

Olympus Corporation of the Americas EasySuite 4K Integrated Operating Room System recall — FDA Z-2233-2024

A subset of the ES4K systems do not have complete records for earth leakage testing. The earth leakage test is a series of measurements intended to…

Class IIclassification
Z-2233-2024official record ID
Jul 10, 2024report date

Recall record at a glance

Official recordZ-2233-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOlympus Corporation of the Americas
Report dateJul 10, 2024
Recall initiation dateApr 24, 2024
Quantity227 units
LocationCenter Valley, PA, United States

Official product description

EasySuite 4K Integrated Operating Room System Model/Catalog Number: EasySuite 4K- The EasySuite 4K system includes a touch panel user interface for quick routing of 2K/4K procedural video to displays within the operating room and for convenient control of room video cameras, surgical cameras, ambient lighting, and surgical lights.

Why the product was recalled

A subset of the ES4K systems do not have complete records for earth leakage testing. The earth leakage test is a series of measurements intended to confirm that the amount of electrical current flowing to the earth is within standard limits

Distribution information

Worldwide distribution - US Nationwide and the countries of Germany, Hong Kong.

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

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About this record

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