Z-3329-2026 Class II Ongoing
FDA device recall Z-3329-2026 was initiated by Olympus Corporation Of The Americas on Aug 27, 2026 and is designated Class II. Reason for recall: While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable. The recall status is ongoing. Affected quantity: 543 cables.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 7, 2026
- Initiation Date
- Aug 27, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 543 cables
Product Description
Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
Reason for Recall
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Distribution Pattern
Worldwide distribution - US Nationwide and the country of Poland.
Code Information
Model Number P580-025, Material Number Material: OS-DPDPC25-G
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-3329-2026
- openFDA file date
- Oct 21, 2026
- Loaded by RegDataLab
- Oct 23, 2026