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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

Nov 2023: 2 reportsDec 2023: 1 reportsJan 2024: 1 reportsFeb 2024: 0 reportsMar 2024: 5 reportsApr 2024: 3 reportsMay 2024: 5 reportsJun 2024: 1 reportsJul 2024: 2 reportsAug 2024: 0 reportsSep 2024: 6 reportsOct 2024: 5 reportsNov 2024: 11 reportsDec 2024: 10 reportsJan 2025: 14 reportsFeb 2025: 3 reportsMar 2025: 15 reportsApr 2025: 10 reportsMay 2025: 16 reportsJun 2025: 5 reportsJul 2025: 14 reportsAug 2025: 6 reportsSep 2025: 19 reportsOct 2025: 9 reportsNov 2025: 11 reportsDec 2025: 10 reportsJan 2026: 10 reportsFeb 2026: 13 reportsMar 2026: 11 reportsApr 2026: 16 reportsMay 2026: 6 reportsJun 2026: 7 reportsJul 2026: 6 reportsAug 2026: 8 reportsSep 2026: 5 reportsOct 2026: 0 reports20242025202619
Last 36 months. The most recent month may be incomplete.

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.

  1. 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.

Recent Xhibit adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Spacelabs Healthcare (Washington), Inc products

All Spacelabs Healthcare (Washington), Inc devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page