CLASS II ONGOING Device recall · Reported 29 Jul 2026 · FDA Enforcement Report

Olympus 4K UHD LCD Monitor recalled by Olympus Corporation of the

Olympus Corporation of the Americas is recalling Olympus 4K UHD LCD Monitor, distributed nationwide in the US. The recall was initiated on 7 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, 7503335.

Quantity recalled10 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2761-2026
FDA event ID: 99288
Recalling firm: Olympus Corporation of the Americas, Center Valley, PA
Classification: Class II
Status: Ongoing
Recall initiated: 7 Jul 2026
FDA classified: 20 Jul 2026
Reported: 29 Jul 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Patient Monitors

Timeline

7 Jul 2026	Recall initiated by company
20 Jul 2026	Classified by FDA	+13 days
29 Jul 2026	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.

Product as listed by the FDA

Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.

Where it was distributed

Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.

Nationwide California Florida New Jersey

Questions about this recall

Why was it recalled?

Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.

Which lots are affected?

Model Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, 7503335.

Where was it sold?

Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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