Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm received reports of telemetry SpO2 numerics...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Spacelabs Healthcare Inc directly.
Affected Products
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.
Quantity: 348 units (292 units in the US and 56 units outside the US)
Why Was This Recalled?
The firm received reports of telemetry SpO2 numerics dropping off the Xhibit Central display. Desaturation, high, and low limit alarms work normally.
Where Was This Sold?
This product was distributed to 27 states: AL, CA, CT, FL, GA, ID, IL, IN, IA, KY, MI, MN, MS, NE, NJ, NY, NC, OH, OK, PA, RI, SC, SD, TX, VA, WA, WY
About Spacelabs Healthcare Inc
Spacelabs Healthcare Inc has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report