Fresh Recalls

FDAClass II · Medical device · Recall Z-2761-2026 · Recalled July 29, 2026

Olympus 4K UHD LCD Monitor recall — Olympus Corporation of the Americas

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Olympus 4K UHD LCD Monitor
Company / brand
Olympus of the Americas
Lot / serial / date codes
Model Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, 7503335.
Distribution
Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Olympus 4K UHD LCD Monitor

3. Open the official notice or contact

Official recall ID
Z-2761-2026
Brand
Olympus of the Americas
Classification
Class II
Units affected
10 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Center Valley, PA, United States
Firm address
3500 Corporate Pkwy, N/A, 18034-8229

Identifying details (verbatim from the notice)

Product codes / lots
Model Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, 7503335.
Distribution
Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
Firm notified the public via
Letter
FDA event ID
99288
Recall initiated
July 7, 2026
FDA classified
July 20, 2026
FDA report date
July 29, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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