Recall Z-3329-2026— Olympus Corporation of the Americas

Name: FDA recall Z-3329-2026
Creator: U.S. Food and Drug Administration
Published: 2026-08-27

Class II · Ongoing

Class II FDA medical device recall by Olympus Corporation of the Americas, initiated 2026-08-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System. Reason: While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable..

Recalling firm: Olympus Corporation of the Americas
Classification: Class II
Status: Ongoing
Initiated: 2026-08-27
Firm location: Center Valley, PA, United States

Product description

Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System

Reason for recall

While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.

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