Class 2 Device Recall Olympus TrippLite

• Date Initiated by Firm: August 27, 2026
• Date Posted: September 29, 2026
• Recall Status: Open, Classified
• Recall Number: Z-3329-2026
• Recall Event ID: 99528
• Product Classification: unknown device name - Product Code N/A
• Product: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
• Code Information: Model Number P580-025, Material Number Material: OS-DPDPC25-G
• FEI Number: 2429304
• Recalling Firm/ Manufacturer: Olympus Corporation of the Americas; 3500 Corporate Pkwy; Center Valley PA 18034-8229
• For Additional Information Contact: Ashley Troiani; 484-5531029
• Manufacturer Reason for Recall: While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
• FDA Determined Cause: Under Investigation by firm
• Action: Consignees were notified on about 08/27/2026 via letter. Consignees were instructed to discontinue using the affected cable, arrange for the replacement of the affected cable, acknowledge receipt of the recall notification through their recall web portal, and forward the notification to other users who may have the affected products, if further transferred.
• Quantity in Commerce: 543 cables
• Distribution: Worldwide distribution - US Nationwide and the country of Poland.

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.