Olympus Tripp-Lite P580-025 DisplayPort Cable May Cause Video Dropout During Use
Olympus recalls 543 P580-025 DisplayPort cables sold worldwide for possible video dropout during high-power operation. Affected cables were sold in the US and Poland. Return or stop using immediately.
Lower-risk recall
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
What happened, in plain English
Olympus is recalling 543 P580-025 DisplayPort cables that may cause video dropout or blackouts when used in high-power mode. This could lead to temporary loss of video signal during normal use. Read more at govinfonow.com/recall/1449231-olympus-corporation-of-the-americas-recalls-olympus-tripp-lite-p580.
Source Summary by GovInfoNow · govinfonow.com/recall/1449231-olympus-corporation-of-the-americas-recalls-olympus-tripp-lite-p580 · Updated October 14, 2026 · FDA enforcement record: FDA #Z-3329-2026
Cite this page
“Olympus Tripp-Lite P580-025 DisplayPort Cable May Cause Video Dropout During Use.” GovInfoNow, updated October 14, 2026. https://govinfonow.com/recall/1449231-olympus-corporation-of-the-americas-recalls-olympus-tripp-lite-p580. Based on FDA recall #Z-3329-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3329-2026%22&limit=1).
Why it’s dangerous
The cable may cause video dropout or blackouts when used in high-power mode with the OLYSENSE Hub System. This happens due to a potential issue with the cable's internal electronics during video transmission.
Who’s affected
Users of the Olympus Tripp-Lite P580-025 25ft DisplayPort cable in the US and Poland are affected. Most at risk are those connecting the cable to OLYSENSE Hub System devices.
How to tell if you have this one
Check for the model number P580-025 on the cable's label. The cable is 25ft long and used with the OLYSENSE Hub System. It was sold in the US and Poland.
- Brand
Olympus- Category
Medical device
What to do — step by step
Check Cable Label
Look for the model number P580-025 on the cable's label to confirm if it's affected.
Stop Using Cable
If the cable has the model number P580-025, stop using it immediately to avoid video dropout.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the country of Poland.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 41 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3329-2026 (August 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3329-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.