Xhibit Exhibit CentralRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10841522100536), received between May 8, 2025 and Sep 24, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “No Audible Alarm” (2 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• MalfunctionJul 3, 2025No Display/Image; No Display/Image

  THE CUSTOMER REPORTED THAT THEY HAD A XHIBIT CENTRAL STATION DISPLAY THAT HAD STOPPED WORKING WHILE BEING USED TO MONITOR PATIENTS. THERE WAS NO PATIENT OR USER HARM ASSOCIATED WITH THIS EVENT. THE CUSTOMER SHIPPED THE DISPLAY TO SPACELABS HEALTHCARE AND IT WAS EVALUATED BY AN EQUIPMENT SERVICE CENTER TECHNICIAN. THE DEVICE WOULD NOT POWER ON. SPACELABS DOES NOT MANUFACTURE THIS PRODUCT; IT WILL BE SENT TO THE OEM FOR REPAIR. 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 22400245 ↗
• MalfunctionMay 8, 2025No Display/Image; No Display/Image

  THE CUSTOMER REQUESTED A DEPOT SERVICE REPAIR FOR A DISPLAY THAT WOULD BLINK AND WOULD NOT PRODUCE AUDIO. THE CUSTOMER SHIPPED THE DISPLAY TO SPACELABS HEALTHCARE FOR EVALUATION. THE DISPLAY WAS RECEIVED AND THE REPORTED PROBLEM WAS NOT VERIFIED. NO MALFUNCTIONS WERE IDENTIFIED. THE DEVICE PASSED ALL TESTING AND WAS RETURNED TO THE CUSTOMER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21990929 ↗

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