Use caution Medical device recall · FDA · Published November 25, 2024

Spacelabs Xhibit Telemetry Receiver Software 1.4.0/1.4.1: Temporary Monitoring Loss Risk

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0810-2025Medical device Spacelabs Healthcare ›

Use caution until it’s fixed

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.

Take action

Contact the company

Recalling firmSpacelabs Healthcare, Inc.35301 Se Center St · Snoqualmie, WA 98065-9216

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/53405-spacelabs-xhibit-telemetry-receiver-software-1-4-0-1-4.

Source Summary by GovInfoNow · govinfonow.com/recall/53405-spacelabs-xhibit-telemetry-receiver-software-1-4-0-1-4 · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0810-2025

Cite this page

“Spacelabs Xhibit Telemetry Receiver Software 1.4.0/1.4.1: Temporary Monitoring Loss Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53405-spacelabs-xhibit-telemetry-receiver-software-1-4-0-1-4. Based on FDA recall #Z-0810-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0810-2025%22&limit=1).

The FDA announced on November 25, 2024, that Spacelabs Healthcare, Inc. is voluntarily recalling the Xhibit Telemetry Receiver with Software, Model 96280, due to a hazard of unsolicited system shutdowns causing temporary loss of patient monitoring.

How to tell if you have it

Brand: Spacelabs Healthcare
Product: Xhibit Telemetry Receiver with Software
Model Number: 96280
Software Versions: 1.4.0 and 1.4.1
UDI-DI: 10841522107177, 10841522100246
Units affected: 434

The hazard

According to the FDA, telemetry receivers with the affected software versions may experience unsolicited system shutdowns and restarts lasting approximately 1 to 1.5 minutes. This results in a temporary loss of monitoring, which could delay necessary clinical intervention if a clinical event occurred during that period.

Context

GovInfoNow's records show Spacelabs Healthcare, Inc. has had 10 other recalls since January 17, 2018. Recent brand recalls include the Xhibit Central Station Model 96102 on June 4, 2026, for audio/video display failures, and the Ultraview SL Command Module Software Recall on March 26, 2026, for electrical leakage risk. Other recent recalls of similar products include GE HealthCare Telemetry Server Recall (April 24, 2026), GE HealthCare CARESCAPE Telemetry Server V5 Recall (April 24, 2026), and GE HealthCare CARESCAPE Telemetry Server ARK-2250L Recall (April 24, 2026).

How to tell if you have this one

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.

Brand
Spacelabs Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Review your device's software version to confirm if it is 1.4.0 or 1.4.1.

Where it went and when

Where it was distributed

Distributed in 26 states and Puerto Rico, and outside the U.S.

FDA distribution: “US: MN, TX, TN, SC, OK, NM, GA, PA, OH, IA, AL, CO, AR, FL, MO, ME, LA, IL, WA, MA, WI, OR, MS, ID, NY, KS, PR. OUS: Canada, Taiwan, Czech Republic, France, Greece, Italy, Kuwait, Philippines, Poland.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arkansas, Colorado, Florida, Georgia, Idaho, Illinois, Iowa, Kansas, Louisiana, Maine, Massachusetts, Minnesota, Mississippi, Missouri, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Washington, Wisconsin.

Recall timeline

FDA published this recall 51 days after the firm started it.

Nov 25, 2024Firm started the recall
Jan 7, 2025FDA classified it Class II
Jan 15, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/53405-spacelabs-xhibit-telemetry-receiver-software-1-4-0-1-4">Spacelabs Xhibit Telemetry Receiver Software 1.4.0/1.4.1: Temporary Monitoring Loss Risk (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-0810-2025 (November 25, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0810-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.