Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to Software related alarm escalation defect occurs after approximately...
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 Telemetry Receiver, Model: 96280
Quantity: 529
Why Was This Recalled?
Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Spacelabs Healthcare, Inc.
Spacelabs Healthcare, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report