Olympus 4K UHD LCD Monitor
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
- Agency
- FDA Device
- Recall date
- Jul 7, 2026
- Status
- Ongoing
- Company
- Olympus Corporation of the Americas
1. What product was recalled?
Olympus 4K UHD LCD Monitor
Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.
Quantity: 10 units
Code or lot text: Model Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474, 7503477, 7503479, 7503263, 7503264, 7503262, 7503261, 7503260, 7503259, 7503335.
- LOT
- 7503259
- LOT
- 7503260
- LOT
- 7503261
- LOT
- 7503262
- LOT
- 7503263
- LOT
- 7503264
- LOT
- 7503335.
- LOT
- 7503477
- LOT
- 7503479
- LOT
- Model Number: OEV321UH. UDI-DI: 04953170418723. Serial Numbers: 7503474
- RECALL-NUMBER
- Z-2761-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
View source evidence for state distribution
- California: Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
- Florida: Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
- New Jersey: Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
- Ohio: Worldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the country of Japan.
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Device source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.