XhibitRecalls & reported problems across all models
Spacelabs Healthcare (Washington), Inc · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 272
- Deaths reported
- 4
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of Xhibit by Spacelabs Healthcare (Washington), Inc in the FDA's device registry (GUDID). Together they are named in 272 adverse event reports in the FDA's MAUDE database, received between Apr 16, 2023 and Sep 24, 2026 — classified as 4 deaths, 268 malfunctions.
The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (82 reports).
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Xhibit recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Aug 30, 2019Class IITerminated
The firm received reports of loss of audio alarm after a power failure or cable disconnection. The loss of audio for a telemetry patient could delay the recognition of an alarm condition.
Z-2261-2020 · Root cause: Software Manufacturing/Software Deployment · Recall details · FDA record ↗
Most reported Xhibit problems
Device problems
- Application Program Freezes or Fails to Launch82
- Unexpected Shutdown75
- No Display/Image46
- Communication or Transmission Problem35
- No Audible Alarm12
- Device Alarm System6
- Display or Visual Feedback Problem4
- Complete Loss of Power3
Patient problems
- No Clinical Signs, Symptoms or Conditions267
- Asystole4
- Arrhythmia1
Xhibit models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Xhibit Xhibit CentralSystem, network and communication, physiological monitors3 deaths218 reports
- Xhibit 96102MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 recall1 death50 reports
- Xhibit Exhibit CentralSYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS4 reports
Recent Xhibit adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890514 ↗MalfunctionSep 24, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890510 ↗MalfunctionSep 24, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890274 ↗MalfunctionSep 24, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890273 ↗MalfunctionSep 10, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50723367 ↗MalfunctionAug 31, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50532751 ↗MalfunctionAug 31, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50532066 ↗MalfunctionAug 31, 2026Insufficient Device Problem Information
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50526120 ↗MalfunctionAug 30, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50512714 ↗MalfunctionAug 13, 2026Unexpected Shutdown
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50242089 ↗MalfunctionAug 13, 2026Intermittent Communication Failure
The customer contacted Spacelabs Healthcare Technical Support to report that while monitoring telemetry patients, the patients would go offline for five to ten seconds every five to ten minutes. There was no report of patient or user harm associated with the event. Spacelabs Technical Support attempted to remotely connect to the Xhibit Telemetry Receives (XTR) however were unable to connect or ping the devices. A Spacelabs Healthcare Product & System Integration Specialist (PSIS) reached out to the customer to attempt to assist with troubleshooting the possible network disruption. At this time, the customer has not responded to the PSIS after numerous attempts. If additional information is made available, a follow-up report will be submitted in accordance with 21 CFR 803.56.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50242085 ↗MalfunctionAug 13, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50242082 ↗MalfunctionAug 8, 2026Application Program Freezes or Fails to Launch
The customer contacted Spacelabs Healthcare to report that while monitoring telemetry patients the Xhibit Central Station (XCS) became unresponsive and patients could no longer be monitored. There was no report of patient or user harm associated with the event. A Spacelabs Technical Support Representative walked the user through performing a hard reboot of the XCS. Following the reboot, the customer confirmed the issue was resolved. Cause of failure was not determined.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50184609 ↗MalfunctionJul 31, 2026No Display/Image
The customer contacted Spacelabs Healthcare Technical Support to report that two Xhibit Central Stations (XCS) went blank at the same time. There was no report of patient or user harm associated with the event. The patients were moved to alternate central stations to resume telemetry monitoring. A Spacelabs Field Service Engineer (FSE) was paged to go on site to assist with troubleshooting. When the FSE reached out to the customer biomed, they stated they were able to resolve the issue, complete details of the resolution were not provided by the customer. The customer stated they were able to resolve the issube after removing power from the displays to reset them. Cause of failure could not be determined.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50095012 ↗MalfunctionJul 27, 2026Communication or Transmission Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50011331 ↗
Other Spacelabs Healthcare (Washington), Inc products
All Spacelabs Healthcare (Washington), Inc devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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