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.
FDA Recall Z-2233-2024 · Posted 2024-06-28
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Recalling FirmOlympus Corporation of the Americas
Recall StatusOpen, Classified
Product CodeNAY
Date Initiated2024-04-24
Product Quantity227 units
Reason for Recall
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
Firm Action
Olympus issued Urgent: Medical Device Corrective Action letter on May 24, 2024
via Courier, 2-day delivery. Letter states reason for recall, health risk and action to take:
An Olympus representative will reach out to you to schedule an on-site service to perform the earth leakage testing on your facility s ES4K system. You may continue to use your ES4K system until an Olympus representative performs the earth leakage test. Additionally, Olympus requires you to take the following actions:
1. Carefully read the content of this notification.
2. If you have further distributed this product, identify your customers, and forward them this notification.
3. Acknowledge receipt of this letter through our Olympus recall portal:
a. Go to https://olympusamerica.com/recall.
b. Enter the recall number "0446
c. Complete the form as instructed and include your account ID number.
4. An Olympus representative will contact you to complete the earth leakage test which will serve as the completion of this field corrective action for your facility.
Olympus requests that you report any complaints, including surgical displays becoming inoperable/unusable or touch current sensation (i.e., vibration, slight tingle), to the Technical Assistance Center (TAC) at 1- 800-848-9024, option 1.
Root Cause
Process control
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Germany, Hong Kong.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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