Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog… — Class II medical device recall Z-2916-2026
Ongoing recall by Spacelabs Healthcare, Inc., reported 2026-08-19, distributed nationwide. Due to off-the-shelf display port component that has audio/video failures
| Recall number | Z-2916-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spacelabs Healthcare, Inc., Snoqualmie, WA, United States |
| Recall initiated | 2026-06-04 |
| Classified | 2026-08-07 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, FR, IT, MY, TH |
| Quantity | 6,074 |
| UPC / GTIN / UDI-DI | 10841522100345 |
| Model numbers | 010-1975-00, 96102 |
Product
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Central Station, Model 96102. Xhibit offers remote surveillance of patient data for those patients connected to a Spacelabs Healthcare bedside monitors and telemetry systems. The DisplayPort audio/video splitter allows users to extend the audio/video source from the Xhibit to additional external displays or monitors. This extension of audio/video is for viewing only and does not allow interaction with the Xhibit. Component: The DisplayPort audio/video splitter is a 3rd party external accessory to Xhibit.
Reason for recall
Due to off-the-shelf display port component that has audio/video failures
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2916-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.