FDA recall, , Moderate risk
Olympus 4K UHD LCD Monitor
The Olympus 4K UHD LCD Monitor can have faulty HDMI and DisplayPort connectors, causing image loss or abnormalities.
Summary by Recall Canary from the FDA notice
What happened
Olympus Corporation of the Americas, located in Center Valley, Pennsylvania, recalled its Olympus 4K UHD LCD Monitor, Model Number OEV321UH, on July 7, 2026. The FDA added the recall to its Enforcement Report on July 20, 2026, and it was in the FDA's weekly enforcement report on July 29, 2026. The recall involved 10 units distributed in California, Florida, New Jersey, Ohio, and Japan.
The agency stated that the HDMI and DisplayPort connectors can become faulty, resulting in image loss or image abnormalities in the electrically powered visual display unit designed for displaying graphical information in color.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and UDI-DI listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Olympus 4K UHD LCD Monitor.
- Model
- OEV321UH
- UDI-DI
- 04953170418723
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of Ohio, California, New Jersey, Florida and the country of Japan.
- Company
- Olympus Corporation of the AmericasCenter Valley, Pennsylvania
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99288
- Recall number
- Z-2761-2026
- Quantity recalled
- 10 units
All recalls from Olympus Corporation of the Americas
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
