Z-3329-2026

Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction...

Name: Z-3329-2026 Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction...
Creator: Olympus Corporation of the Americas
Published: 2026-08-27
License: https://open.fda.gov/license/

Olympus Corporation of the Americas / initiated 2026-08-27 / Open, Classified

FDA source

Recall record

Recall number: Z-3329-2026
Status: Open, Classified
Initiated: 2026-08-27
Posted: 2026-09-29
Recalling firm: Olympus Corporation of the Americas
Product: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
Product code: N/A
Reason for recall: While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
FDA root 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.
Product codes and lots: Model Number P580-025, Material Number Material: OS-DPDPC25-G

Product code N/A

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-10-02. View this recall on fda.gov (opens on fda.gov)