Recall Z-2761-2026— Olympus Corporation of the Americas

Name: FDA recall Z-2761-2026
Creator: U.S. Food and Drug Administration
Published: 2026-07-07

Class II · Ongoing

Class II FDA medical device recall by Olympus Corporation of the Americas, initiated 2026-07-07. It names one FDA 510(k) clearance: K220069. Product: Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.. Reason: Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities..

Recalling firm: Olympus Corporation of the Americas
Classification: Class II
Status: Ongoing
Initiated: 2026-07-07
Firm location: Center Valley, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K220069 — 4K UHD LCD Monitor OEV321UHOlympus Medical Systems Corp.·cleared 2022-03-09

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.