Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENS
Summary
The FDA issued a Class II for Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an ac by Olympus Corporation of the Americas. Reason: While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable..
Details
Source
Device Recall
External ID
Z-3329-2026
Action Date
2026-10-07
Status
Ongoing
Category
device
Product Description
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
Lot/Code Info: Model Number P580-025, Material Number Material: OS-DPDPC25-G
Quantity Affected: 543 cables
Reason for Recall
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Distribution
Worldwide distribution - US Nationwide and the country of Poland.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-27
Company
Center Valley, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 238 device recalls issued in the same week, part of 518 device-related FDA actions this month.
Olympus Corporation of the Americas has 336 FDA actions in our database, including 336 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Olympus Corporation of the Americas) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Olympus Corporation of the Americas have FDA actions?
Olympus Corporation of the Americas has 336 FDA actions in our database, including 336 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-3329-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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