Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U
FDA Recall Z-0264-2025 · Posted 2024-10-30
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Recalling FirmOlympus Corporation of the Americas
Recall StatusOpen, Classified
Product CodeGEI
Date Initiated2024-09-04
Product Quantity279 units
Reason for Recall
There was an increase in complaints indicating an occurrence of system error E1226 "Could not write to Audio Buffer" during procedures using the ESG-410 (SEP).
Firm Action
An URGENT: MEDICAL DEVICE CORRECTIVE ACTION notification letter dated 10/1/24 was sent to customers.
Actions Required:
Our records indicate that your facility has received one or more affected ESG-410 (SEP) units.
An Olympus representative will reach out to you to coordinate a mutually convenient time to complete a software update on your affected ESG-410 (SEP) unit(s). You may continue to use your ESG-410 (SEP) generator until the software update is completed. Additionally, Olympus requires you to take the following actions:
1. Carefully read the content of this notification.
2. Olympus requests that you acknowledge receipt of this letter. Access the Olympus recall portal to indicate that you have received this notification.
" Go to https://olympusamerica.com/recall
Enter the recall number "0457
" Complete the form as instructed.
3. Olympus s record of the completed software upgrade to your ESG-410 (SEP) generator(s) will serve as the acknowledgment of this field corrective action for your facility
4. If you have further distributed this product, identify your customers, and forward them this notification.
Olympus requests that you report any complaints, including the ESG-410 generator system error E1226 "Could not write to Audio Buffer , or any associated injuries to the Technical Assistance Center (TAC) at 1- 800-848-9024, option 1, and the FDA.
If you require additional information, please do not hesitate to contact me directly by phone at (647) 999-3203 or by e-mail at [email protected].
Root Cause
Software design
Distribution Pattern
US Nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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