Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR) Recalled by Spacelabs Healthcare Inc Due to Reports of an abnormally high frequency of squelch...
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
The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280 is used to transmit patient(s) physiological measurements and data to a monitor.
Quantity: 217 units of XTRs and 531 units of PCBAs (164 XTRs and 425 PCBAs in US and 53 XTRs and 106 PCBAs outside the US)
Why Was This Recalled?
Reports of an abnormally high frequency of squelch events on Xhibit Telemetry Receivers (XTR), which is indicative of the loss of the telemetry data signal. In some cases, the Xhibit Central Monitor was also reported to display an Xhibit Offline error message for all patients being monitored.
Where Was This Sold?
This product was distributed to 17 states: AL, AZ, CA, CO, CT, FL, ID, IN, KY, MI, MN, MS, MO, MT, SC, TX, 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