Olympus Corporation Of The Americas recalls Olympus Tripp-Lite P580-025 25ft DisplayPort Cable
Reason for recall
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub SystemModel Number
What the firm is doing
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.
DistributionShow detailsHide
Worldwide distribution - US Nationwide and the country of Poland.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-3329-2026
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Olympus Corporation of the AmericasSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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