RecallReported October 7, 2026
Class II recall by Olympus Corporation of the Americas
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
FDA's enforcement report of October 7, 2026 lists a Class II recall by Olympus Corporation of the Americas of Center Valley, PA. Product: Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System. Status: Ongoing.
On the record
- Recalling firm
- Olympus Corporation of the Americas
- Location
- Center Valley, PA
- Classification
- Class II
- Status
- Ongoing
- Recall number
- Z-3329-2026
- Product type
- Devices
- Recall initiated
- 2026-08-27
- Reported by FDA
- 2026-10-07
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
More
Watch Olympus Corporation of the Americas
A free account shows the last 7 days of every FDA, SEC and ClinicalTrials.gov source. Pro adds a watchlist: one email when FDA acts on a company you name.
From FDA enforcement reports. The record may have changed since it was read.
Approve Suite is not affiliated with FDA, or with Olympus Corporation of the Americas. Informational only.
See something wrong on this page? Write to info@approvesuite.com and we will check it against the source. How corrections work.