Olympus 4K UHD LCD Monitor Recall Issued
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Olympus Corporation of the Americas is recalling 10 units of the OEV321UH 4K UHD LCD Monitor due to potential faulty HDMI and DisplayPort connectors.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 12, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Olympus Corporation of the Americas initiated a voluntary recall of certain Olympus 4K UHD LCD Monitors after identifying a potential issue with the HDMI and DisplayPort connectors that can become faulty, resulting in image loss or image abnormalities.
Which Products Are Affected
The recall involves the Olympus 4K UHD LCD Monitor, Model Number OEV321UH, with UDI-DI 04953170418723. Affected serial numbers are: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, and 7503335. A total of 10 units are affected. Distribution includes US nationwide in the states of OH, CA, NJ, FL, and Japan.
What You Should Do
Consumers in possession of an affected unit should contact Olympus Corporation of the Americas for further information regarding the recall.
Why This Matters
The recall affects a small number of medical display devices distributed in multiple states and internationally, with the potential for image abnormalities during use.
Source
FDA recall number Z-2761-2026 (Class II, event ID 99288).
Original source: FDA Official Notice ↗
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