Spacelabs Healthcare recall: Xhibit Central Station
Spacelabs Healthcare, Inc. is recalling Xhibit Central Station – 6074. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on June 4, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Xhibit Central Station |
| Brand | Spacelabs Healthcare |
| Company | Spacelabs Healthcare, Inc. |
| Type | Medical devices |
| Classification | Class II |
| Recall date | June 4, 2026 |
| Published by FDA | August 19, 2026 |
| Quantity | 6074 |
| Recall ID | 99260 |
Recalled products
- 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.
- FDA recall number
- Z-2916-2026
- Codes, lots and dates
- Model/Catalog Number: 96102 DisplayPort Splitter Part Number: 010-1975-00 UDI-DI codes: 1084152212706 10841522100345 Serial Numbers: Pending
- Quantity
- 6074
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99260
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Snoqualmie, WA, United States
Why it was recalled
The reason the FDA lists: “Due to off-the-shelf display port component that has audio/video failures”
Where it was sold
Nationwide. Distribution as the FDA records it: “Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, VA, WA, WI, WY and the countries of CANADA, FRANCE, ITALY, MALAYSIA, THAILAND.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99260, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is Spacelabs Healthcare Xhibit Central Station recalled?
Yes. Spacelabs Healthcare, Inc. recalled it on June 4, 2026; FDA published it August 19, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Due to off-the-shelf display port component that has audio/video failures
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.