Lower riskMedical device recall · FDA · Published July 7, 2026
Olympus 4K UHD Monitor Recall: HDMI/DP Connectors May Cause Image Loss
Olympus recalls 4K UHD LCD monitors (model OEV321UH) due to HDMI and DisplayPort connectors potentially causing image loss or abnormalities. Affected units have specific serial numbers.
“Olympus 4K UHD Monitor Recall: HDMI/DP Connectors May Cause Image Loss.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/127762-olympus-4k-uhd-monitor-recall-hdmi-dp-connectors-may-cause. Based on FDA recall #Z-2761-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2761-2026%22&limit=1).
The FDA announced on July 7, 2026, that Olympus Corporation of the Americas is recalling its 4K UHD LCD Monitor, model OEV321UH. The agency cited a potential for faulty HDMI and DisplayPort connectors causing image loss or abnormalities.
The recall addresses the potential for HDMI and DisplayPort connectors to become faulty. This defect can result in image loss or image abnormalities on the display.
Context
GovInfoNow's records show Olympus Corporation of the Americas has 133 other recalls on record since August 18, 2017. Other recent recalls by the brand include the Olympus Tripp-Lite P580-025 DisplayPort Cable (August 27, 2026), the Olympus M3 Gold Autoclavable Lateral Telescope 70 (August 24, 2026), and the BiCOAG Hemostasis Probe 7Fr Connector (August 19, 2026). Other recent recalls of similar products include the Philips Allura Xper FD10 System (April 30, 2026), the Olympus OER-Pro (October 31, 2025), and the Olympus OER-Elite (October 31, 2025).
How to tell if you have this one
Check for the model number OEV321UH on your monitor. Affected units have serial numbers including 7503474, 7503477, and others listed in the recall notice.
Brand
Olympus
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Monitor Model
Verify your monitor's model number is OEV321UH to determine if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, New Jersey, Ohio.
Recall timeline
FDA published this recall 22 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2761-2026 (July 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2761-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.