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

Spacelabs Xhibit Telemetry Receiver Model 96280: Temporary Monitoring Loss Risk

Spacelabs Healthcare recalls Xhibit Telemetry Receiver Model 96280 due to temporary system shutdowns causing potential delays in detecting clinical events. Affected units may lose monitoring for 1-1.5 minutes during Windows proxy issues.

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

🇺🇸 FDA recall #Z-0809-2025Medical device Spacelabs Healthcare ›

Use caution until it’s fixed

Telemetry receiver systems may experience a Windows proxy Issue causing the system to 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; 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 is recalling Xhibit Telemetry Receiver Model 96280 units that may shut down temporarily, causing brief loss of patient monitoring. This could delay detection of critical clinical events if they occur during the shutdown period. Read more at govinfonow.com/recall/53397-spacelabs-xhibit-telemetry-receiver-model-96280-temporary-monitoring-loss-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/53397-spacelabs-xhibit-telemetry-receiver-model-96280-temporary-monitoring-loss-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0809-2025

Cite this page

“Spacelabs Xhibit Telemetry Receiver Model 96280: Temporary Monitoring Loss Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53397-spacelabs-xhibit-telemetry-receiver-model-96280-temporary-monitoring-loss-risk. Based on FDA recall #Z-0809-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0809-2025%22&limit=1).

The FDA announced on Nov. 25, 2024, that Spacelabs Healthcare, Inc. is recalling the Xhibit Telemetry Receiver, Model 96280, due to a hazard that may cause temporary loss of patient monitoring. The agency issued recall number Z-0809-2025 for the voluntary Class II action affecting 2,265 units distributed in the U.S. and internationally.

How to tell if you have it

Brand: Spacelabs Healthcare
Product: Xhibit Telemetry Receiver with Service Manual
Model: 96280
Service Manuals P/N: 070-2409-07 and Prior
UDI-DI: 10841522107177, 10841522100246

The hazard

According to the FDA, telemetry receiver systems may experience a Windows proxy issue causing the system to shut down and restart for approximately 1 to 1.5 minutes. This results in an Offline display and 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 10 other recalls on record since Jan. 17, 2018. Recent brand recalls include the Spacelabs Xhibit Central Station Model 96102 (June 4, 2026) for audio/video display failures, the Spacelabs Ultraview SL Command Module Software Recall (March 26, 2026) for electrical leakage risk, and the Spacelabs Healthcare Multi-parameter Command Module Model 91496 Recall (Feb. 27, 2026) for inaccurate cardiac output readings. Other recent recalls of similar products include the GE HealthCare Telemetry Server Recall (April 24, 2026), the GE HealthCare CARESCAPE Telemetry Server V5 Recall (April 24, 2026), and the GE HealthCare CARESCAPE Telemetry Server ARK-2250L Recall (April 24, 2026).

How to tell if you have this one

Check for the Xhibit Telemetry Receiver Model 96280 with Service Manual. Units sold with UDI-DI numbers 10841522107177 or 10841522100246 are affected.

Brand
Spacelabs Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check System Status
Monitor for temporary shutdowns (1-1.5 minutes) causing loss of monitoring, which may indicate the issue.

Where it went and when

Where it was distributed

Distributed in 43 states and Puerto Rico, and outside the U.S.

FDA distribution: “US: OK, MN, IA, SC, NE, MI, NY, KY, GA, MO, MT, LA, WA, SD, CO, PA, WY, TX, ID, NJ, FL, OH, MS, OR, AK, IL, AR, KS, AL, TN, WI, VA, NM, CA, IN, RI, NV, MA, NC, ME, CT, AZ, MD, PR. OUS: Kuwait, Australia, Canada, Roumanie, Greece,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin, Wyoming.

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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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/53397-spacelabs-xhibit-telemetry-receiver-model-96280-temporary-monitoring-loss-risk">Spacelabs Xhibit Telemetry Receiver Model 96280: 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-0809-2025 (November 25, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0809-2025 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.