CLASS II ONGOING Device recall · Reported 7 Oct 2026 · FDA Enforcement Report
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recalled
Olympus Corporation of the Americas is recalling Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, distributed nationwide in the US. The recall was initiated on 27 Aug 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-3329-2026
- FDA event ID
- 99528
- Recalling firm
- Olympus Corporation of the Americas, Center Valley, PA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 27 Aug 2026
- FDA classified
- 29 Sep 2026
- Reported
- 7 Oct 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 27 Aug 2026 | Recall initiated by company | |
| 29 Sep 2026 | Classified by FDA | +33 days |
| 7 Oct 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Product as listed by the FDA
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
Where it was distributed
Worldwide distribution - US Nationwide and the country of Poland.
Questions about this recall
Why was it recalled?
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Which lots are affected?
Model Number P580-025, Material Number Material: OS-DPDPC25-G
Where was it sold?
Worldwide distribution - US Nationwide and the country of Poland.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 13 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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