Lower riskMedical device recall · FDA · Published June 4, 2026
Spacelabs Xhibit Central Station Model 96102: Audio/Video Display Failures
Spacelabs recalls Xhibit Central Station Model 96102 due to audio/video failures in the DisplayPort splitter component. Affected units may show distorted or no video output.
“Spacelabs Xhibit Central Station Model 96102: Audio/Video Display Failures.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459601-spacelabs-xhibit-central-station-model-96102-audio-video-display-failures. Based on FDA recall #Z-2916-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2916-2026%22&limit=1).
The FDA announced on June 4, 2026, that Spacelabs Healthcare is recalling the Xhibit Central Station, Model 96102, due to off-the-shelf display port components causing audio/video failures. This voluntary Class II recall affects 6,074 units distributed worldwide.
How to tell if you have it
Brand: Spacelabs
Product Name: Xhibit Central Station
Model/Catalog Number: 96102
DisplayPort Splitter Part Number: 010-1975-00
UDI-DI codes: 1084152212706, 10841522100345
The hazard
The recall is due to an off-the-shelf display port component that has audio/video failures. The DisplayPort audio/video splitter is a third-party external accessory to the Xhibit.
Context
GovInfoNow's records show Spacelabs Healthcare, Inc. has 10 other recalls on record since January 17, 2018. Other recent recalls of similar products include Spacelabs Ultraview SL Command Module Software Recall (March 26, 2026), Spacelabs Healthcare Multi-parameter Command Module Model 91496 Recall (February 27, 2026), and Spacelabs DVI Display Cables Recall (September 5, 2025).
How to tell if you have this one
Check for the model number 96102 on the Xhibit Central Station. The DisplayPort splitter part number is 010-1975-00. Units sold with this model number are affected.
Brand
Spacelabs
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check DisplayPort Splitter
Inspect the DisplayPort splitter for audio/video failures. If displays show distorted or no video, stop using the splitter.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 44 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “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…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2916-2026 (June 4, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2916-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.