Ultraview SLRecalls & reported problems across all models

We found 2 models of Ultraview SL by Spacelabs Healthcare (Washington), Inc in the FDA's device registry (GUDID). Together they are named in 5 adverse event reports in the FDA's MAUDE database, received between Dec 5, 2024 and Feb 19, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Communication or Transmission Problem” (2 reports).

2 FDA recall records name at least one of these models by its device identifier, 2 still open.

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

Ultraview SL 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. Mar 26, 2026Open, Classified

   Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).

   Z-2052-2026 · Root cause: Process control · Recall details · FDA record ↗

2. Feb 27, 2026Open, Classified

   Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, which may result in inaccurate readings, or the need of additional readings, which may lead to delayed care and/or fluid overload.

   Z-1793-2026 · Root cause: Component change control · names 2 of these models · Recall details · FDA record ↗

Most reported Ultraview SL problems

Ultraview SL models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Ultraview SL Ultraview SL®

  SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
  2 recalls2 reports
• Ultraview SL UV SL Command Module

  DETECTOR AND ALARM, ARRHYTHMIA
  1 recall3 reports

Recent Ultraview SL adverse event reports

The 5 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionFeb 19, 2026Device Sensing Problem

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TO REPORT THAT THEIR SPACELABS ULTRAVIEW SL COMMAND MODULE FAILED TO DETECT THAT A PATIENT WAS EXPERIENCING VENTRICULAR TACHYCARDIA. NO PATIENT OR USER HARM WAS REPORTED. THE USER WAS ADVISED TO SWAP THE MODULE FOR A KNOWN WORKING MODULE. MULTIPLE UNSUCCESSFUL ATTEMPTS TO FOLLOW UP WITH THE CUSTOMER WERE MADE. 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 24397729 ↗
• MalfunctionFeb 6, 2026Intermittent Communication Failure

  THE CUSTOMER CONTACTED SPACELABS HEALTHCARE TO REPORT THAT PATIENT PARAMETERS WERE INTERMITTENTLY DROPPED WHILE A ULTRAVIEW COMMAND MODULE WAS IN USE. THERE WAS NO PATIENT OR USER HARM ASSOCIATED WITH THIS EVENT. THE CUSTOMER'S BIOMED EVALUATED THE REPORTED ISSUE AND FOUND THAT THE PINS OF THE COMMAND MODULE WERE BENT AND PUSHED IN. THE BIOMED READJUSTED THE PINS AND CONFIRMED THAT THE ISSUE WAS RESOLVED. THE CAUSE OF THE REPORTED ISSUE WAS DUE TO BENT PINS ON THE COMMAND MODULE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24284993 ↗
• MalfunctionSep 2, 2025Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch

  THE CUSTOMER REPORTED THAT WHILE MONITORING PATIENTS, THE MODULE WOULD INTERMITTENTLY LOSE WAVEFORMS. CLINICAL STAFF WOULD RESET THE MONITOR TO GET VITALS TO RESUME. THE CUSTOMER REPORTED THAT THEY MOVED THE PATIENT TO A NEW PATIENT MONITOR. THE CUSTOMER WAS ADVISED TO REACH OUT TO THEIR INTERNAL BIOMED TEAM TO EVALUATE THE DEVICE. AT THIS TIME, THE CUSTOMER HAS NOT RESPONDED TO ATTEMPTS TO GET ADDITIONAL INFORMATION. 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 22949025 ↗
• MalfunctionDec 6, 2024Communication or Transmission Problem; Communication or Transmission Problem

  THE CUSTOMER REPORTED THAT WHILE IN USE, THE UVSL COMMAND MODULE LOST THE ABILITY TO MONITOR PATIENT PARAMETERS. THERE WAS NO PATIENT OR USER HARM ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20860842 ↗
• MalfunctionDec 5, 2024Communication or Transmission Problem; Communication or Transmission Problem

  THE CUSTOMER REPORTED THAT WHILE IN USE, THE UVSL COMMAND MODULE STOPPED MONITORING PATIENT PARAMETERS. THERE WAS NO PATIENT OR USER HARM ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20858714 ↗

Other Spacelabs Healthcare (Washington), Inc products

• Xhibit3 models · 272 reports · 1 recall
• qube2 models · 24 reports · 3 recalls
• Xprezzon2 models · 5 reports · 3 recalls