Olympus Tripp-Lite DisplayPort Cables
The DisplayPort cable may cause a video dropout or blackout in high-power mode.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Olympus Corporation of the Americas began a recall on August 27, 2026, of the Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used with the OLYSENSE Hub System. The FDA added the recall to its Enforcement Report on September 29, 2026. The recall involves 543 cables because, in high-power operating mode, a video dropout or blackout may occur when using this accessory cable.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the listed under your product.
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable
Details
- Company began the recall
- Sold in
Worldwide distribution - US Nationwide and the country of Poland.
- Event ID
- 99528
- Recall No.
- Z-3329-2026
- Company
- Olympus Corporation of the AmericasCenter Valley, Pennsylvania
- Hazard
- Device defect
- Quantity recalled
- 543 cables
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
Summary updated
In FDA's weekly enforcement report
