Olympus Corporation of the Americas 2025-08-27 Health serious FDA
Health · FDA · Recall #FDA-Z-2338-2025
Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator… Recall
Issued August 27, 2025 · Olympus Corporation of the Americas
In August 2025, Olympus Corporation of the Americas recalled the Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.
What you should do
- 1 Stop using Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Olympus Corporation of the Americas to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Olympus Corporation of the Americas
- Category
- Health
- Recall date
- August 27, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2338-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Olympus Corporation of the Americas has 42 recalls in our database, including 6 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.