Xhibit Xhibit CentralRecalls & reported problems

Summary

The FDA's MAUDE database contains 218 adverse event reports that list this exact device (DI 10841522127069), received between Apr 16, 2023 and Sep 24, 2026 — classified as 3 deaths, 215 malfunctions.

The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (69 reports).

5 other recalls cover devices cleared under the same FDA submission (K122146); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 218 reports, 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 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 ↗
• MalfunctionJul 27, 2026No Audible Alarm

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50011328 ↗
• MalfunctionJul 16, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25850453 ↗
• MalfunctionJul 10, 2026No Display/Image

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25781301 ↗
• MalfunctionJul 2, 2026Communication or Transmission Problem

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TO REPORT THAT THEIR XHIBIT CENTRAL STATION LOST ALL TELEMETRY MONITORING FOR TWELVE MINUTES BEFORE RETURNING ON ITS OWN. ADDITIONAL INFORMATION WAS REQUESTED FROM THE CUSTOMER TO DETERMINE CAUSE OF FAILURE, HOWEVER AT THIS TIME, THE CUSTOMER HAS NOT RESPONDED. 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 25700104 ↗
• MalfunctionJun 18, 2026Communication or Transmission Problem

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT THE XHIBIT CENTRAL STATION (XCS) WAS GOING OFFLINE FOR ALL BEDS FOR TEN MINUTES BEFORE RETURNING ON ITS OWN. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. SPACELABS TECHNICAL SUPPORT ADVISED THE CUSTOMER THAT THE ISSUE INDICATED A POSSIBLE NETWORK PROBLEM AND TO REACH OUT TO THEIR INTERNAL NETWORKING TEAM. AT THIS TIME ADDITIONAL INFORMATION IS NOT AVAILABLE. 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 25553642 ↗
• MalfunctionJun 12, 2026Communication or Transmission Problem

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT WHILE MONITORING TELEMETRY PATIENTS ON A XHIBIT CENTRAL STATION, ALL TELEMETRY PATIENTS DROPPED. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. THE LOSS OF COMMUNICATION LASTED A FEW MINUTES BEFORE RETURNING ON ITS OWN. THE ISSUE WAS ESCALATED TO A SPACELABS HEALTHCARE PRODUCT SUPPORT SPECIALIST (PSS) TO DETERMINE ROOT CAUSE. THE PSS REQUESTED A FIELD SERVICE ENGINEER TO GO ON SITE AND GET LOGS. AT THIS TIME, THE LOGS HAVE NOT BEEN RECEIVED. A FOLLOW-UP REPORT WILL BE SUBMITTED IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25494196 ↗
• MalfunctionJun 4, 2026Display or Visual Feedback Problem

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT AFTER AN ACCIDENTAL RESTART ON THE XHIBIT CENTRAL STATION (XCS) THE RESOLUTION WAS INCORRECT. THE INCORRECT RESOLUTION MADE IT DIFFICULT FOR CLINICAL STAFF TO MONITOR PATIENTS. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. THE CUSTOMER ATTEMPTED A SOFTWARE RESTART, A FULL SYSTEM REBOOT, AND RESEATING THE DISPLAY CABLES, HOWEVER THE ISSUE WAS NOT RESOLVED. THE CUSTOMER DECLINED SUPPORT FROM FIELD SERVICE AND STATED THEY WOULD REACH OUT TO THEIR INTERNAL BIOMED TEAM. THE CUSTOMER HAS NOT RESPONDED TO MULTIPLE ATTEMPTS TO GET ADDITIONAL INFORMATION AND CONFIRMATION OF RESOLUTION. 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 25401838 ↗
• MalfunctionJun 4, 2026No Display/Image

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT THE DISPLAY OF THE XHIBIT CENTRAL STATION (XCS) WAS BLANK AND SEARCHING FOR A VGA VIDEO SIGNAL. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. THE CUSTOMER BIOMED STATED THAT THEY ALREADY ATTEMPTED TO POWER CYCLE THE DISPLAY, HOWEVER THE ISSUE REMAINED. A SPACELABS FIELD SERVICE ENGINEER (FSE) WAS PAGED, HOWEVER, BEFORE THE FSE WENT ON SITE, THE CUSTOMER INFORMED THE FSE THEY RESOLVED THE ISSUE BY REPLACING THE DISPLAY AND NO FURTHER ASSISTANCE WAS NEEDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25401837 ↗
• MalfunctionJun 4, 2026Unexpected Shutdown

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT A XHIBIT CENTRAL STATION (XCS) THAT MONITORS TELEMETRY PATIENTS SHUT DOWN ON ITS OWN TWICE. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. THE CUSTOMER REPORTED THAT AFTER THE SECOND SHUT DOWN, THE DEVICE WAS FUNCTIONAL WITH NO FURTHER ISSUES. THE CUSTOMER WAS ADVISED TO SEND THE DEVICE IN FOR SERVICE. THE CUSTOMER HAS AN OPEN RMA TO SHIP THE UNIT IN FOR REPAIR. AT THIS TIME THE DEVICE HAS NOT BEEN RECIEVED. A FOLLOW-UP REPORT WILL BE SUBMITTED IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25401836 ↗
• MalfunctionMay 28, 2026No Display/Image; Unexpected Shutdown

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TO REQUEST A DEPOT REPAIR FOR A XHIBIT CENTRAL STATION (XCS) THAT WAS HAVING DISPLAY ISSUES AND WOULD OVERHEAT AND SHUT DOWN. THE DEVICE HAS BEEN RECEIVED, HOWEVER, AT THIS TIME REPAIR HAS NOT YET BEEN COMPLETED. A FOLLOW-UP REPORT WILL BE SUBMITTED IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25325269 ↗
• MalfunctionMay 28, 2026No Display/Image

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TECHNICAL SUPPORT TO REPORT THAT ON THEIR XHIBIT CENTRAL STATION (XCS) ALL FOUR DISPLAYS AND REMOTE DISPLAYS WENT BLANK. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. TECHNICAL SUPPORT ADVISED THE CUSTOMER REACH OUT TO THEIR INTERNAL BIOMED TEAM TO RESOLVE THE ISSUE. IN A FOLLOW UP CALL, IT WAS STATED THAT THE ISSUE WAS RESOLVED BY AN IT REP POWER CYCLING THE XCS. CAUSE OF FAILURE WAS NOT IDENTIFIED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25325268 ↗
• MalfunctionMay 15, 2026Unexpected Shutdown

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TO REQUEST DEPOT REPAIR FOR A XHIBIT CENTRAL STATION (XCS) THAT WAS RANDOMLY SHUTTING DOWN ON ITS OWN. THERE WAS NO REPORT OF PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. A RETURN AUTHORIZATION WAS GENERATED FOR THE CUSTOMER TO RETURN THE UNIT, HOWEVER, THE CUSTOMER LATER CALLED BACK AND CANCELLED THE SERVICE REQUEST. THE CUSTOMER REPORTED THAT THEY HAD CLEANED OUT THE UNIT, IT NO LONGER EXPERIENCED THE UNEXPECTED SHUT DOWNS AND THAT A REPAIR WAS NO LONGER NEEDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25193012 ↗
• MalfunctionMay 7, 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 25116427 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K122146. One submission often covers many models, so check the product and lot details in each record.

• Z-2916-2026 · Jun 4, 2026 · Open, Classified
  Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Central S
• Z-2261-2020 · Aug 30, 2019 · Terminated
  Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected t
• Z-0332-2017 · Oct 18, 2016 · Terminated
  Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to network
• Z-2885-2016 · Aug 25, 2016 · Terminated
  Spacelabs Healthcare Xhibit Central Station, Model 96102, Version 1.1.2. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient
• Z-1092-2016 · Feb 26, 2016 · Terminated
  Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of patient data for those patients connected to networked Spacelabs H