FDA Recall Open, Classified

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.

Recall: Z-2233-2024 · Initiated April 24, 2024

Recall

Recall Number
Z-2233-2024
Event Number
94711
Firm
Olympus Corporation of the Americas
FEI Number
2429304
Product Code
NAY
Status
Open, Classified
Root Cause
Process control
Initiated
April 24, 2024
Posted
June 28, 2024
Address
3500 Corporate Pkwy, Center Valley, PA, 18034-8229

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.

Reason

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

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.

Distribution

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

Quantity

227 units