Ultraview SL UV SL Command ModuleRecalls & reported problems
Spacelabs Healthcare (Washington), Inc · OPTION, MASIMO SET SPO2 · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10841522106415), received between Dec 5, 2024 and Feb 19, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Communication or Transmission Problem” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
13 other recalls cover devices cleared under the same FDA submission (K103142); 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.
Reports received per month
Recalls naming this device
- 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 · FDA record ↗
Most reported problems
Device problems
- Communication or Transmission Problem2
- Device Sensing Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, 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 ↗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 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K103142. One submission often covers many models, so check the product and lot details in each record.
- Z-2245-2026 · Apr 24, 2026 · Open, ClassifiedGE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor,
- Z-2244-2026 · Apr 24, 2026 · Open, ClassifiedGE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With A
- Z-2243-2026 · Apr 24, 2026 · Open, ClassifiedGE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, P
- Z-2247-2026 · Apr 24, 2026 · Open, ClassifiedGE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patie
- Z-2246-2026 · Apr 24, 2026 · Open, ClassifiedGE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v
- Z-2052-2026 · Mar 26, 2026 · Open, ClassifiedBrand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software Version: N/A Product Description: The Command Module (91496)
- Z-1503-2023 · Apr 12, 2023 · Open, ClassifiedUltraview SL (UVSL) Command Module, Model 91496
- Z-2343-2016 · Jul 1, 2016 · Terminated91496 Ultraview SL Command Module, Options A, B, C, and I. Option A: ECG/Respiration, SpO2, Temperature x2 & adult/neonate NIBP. Option B: ECG/Respiration, Invasive Pressure x2,
- Z-1577-2015 · Apr 21, 2015 · TerminatedUltraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management S
- Z-1542-2015 · Apr 17, 2015 · TerminatedUltraview SL Command Modules, Model 91496-M, upgraded with the Masimo SpO2 Option. Product Usage: The Spacelabs Multi-parameter Module is intended for use with the Patient Care M
- Z-1705-2014 · May 8, 2014 · TerminatedSpacelabs Medical Ultraview SL Command Module, Model 91496. Arrhythmia Detector and Alarm. The Multi-parameter Module is used with the Patient Care Management System (PCMS) to a
- Z-0690-2012 · Nov 3, 2011 · TerminatedUltraview SL Command Module is the Spacelabs Multi-parameter Module. It is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various
- Z-0776-2012 · Jul 13, 2011 · TerminatedSpacelabs Medical Ultraview SL Command Module, Model 91496. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, mon
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.