FDA recall, , Moderate risk
Xhibit Central Station
The Xhibit Central Station has audio/video failures due to a display port component.
Summary by Recall Canary from the FDA notice
What happened
Spacelabs Healthcare, Inc., of Snoqualmie, Washington, began a recall on June 4, 2026, of the Xhibit Central Station, Model 96102, because an off-the-shelf display port component has audio/video failures.
The product offers remote surveillance of patient data for patients connected to Spacelabs bedside monitors and telemetry systems, and the DisplayPort audio/video splitter allows users to extend the audio/video source to additional external displays.
The recall was added to the FDA's Enforcement Report on August 7, 2026, and distributed nationwide in the U.S. and to Canada, France, Italy, Malaysia, and Thailand.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number matches.
Xhibit Central Station
- Model number
- 96102
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of Alaska, Alabama, Arkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, PR, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin, Wyoming and the countries of CANADA, FRANCE, ITALY, MALAYSIA, THAILAND.
- Company
- Spacelabs Healthcare, Inc.Snoqualmie, Washington
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99260
- Recall number
- Z-2916-2026
All recalls from Spacelabs Healthcare, Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
