Spacelabs Healthcare recalls Xhibit Telemetry Receiver software versions 1.4.0 and 1.4.1 that may cause temporary monitoring loss during system shutdowns, risking delayed clinical interventions. Affected units have specific UDI-DI codes.
Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.
Spacelabs Healthcare recalls Xhibit Telemetry Receivers with software versions 1.4.0 and 1.4.1. These devices may shut down unexpectedly for 1-1.5 minutes, causing temporary loss of patient monitoring that could delay critical clinical responses if an event occurs during the outage.
The affected software versions cause the device to shut down unexpectedly for 1 to 1.5 minutes. During this time, patient monitoring is lost, which could delay critical clinical interventions if an event occurs while the system is offline.
Healthcare facilities using Spacelabs Xhibit Telemetry Receivers with software versions 1.4.0 or 1.4.1 are most at risk. Staff monitoring patients with these devices could face delayed detection of clinical events during temporary system outages.
Check for software versions 1.4.0 or 1.4.1 on your Spacelabs Xhibit Telemetry Receiver. Affected units have UDI-DI codes 10841522107177 or 10841522100246.
Review your device's software version to confirm if it is 1.4.0 or 1.4.1.
Software versions 1.4.0 and 1.4.1.
The device may shut down unexpectedly for 1-1.5 minutes, causing temporary loss of monitoring that could delay detection of clinical events if they occur during the outage.
UDI-DI codes 10841522107177 and 10841522100246.
We’ve drafted a message you can send Spacelabs Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0810-2025 — Spacelabs Healthcare Spacelabs Healthcare Hello, I own a Spacelabs Healthcare that is covered by recall Z-0810-2025 from Spacelabs Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
