The Recall Desk

Manufacturer

Spacelabs Healthcare, Inc.

31 recalls in our database name Spacelabs Healthcare, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
31
Critical
0
Severe
2
Most recent
2026-08-19

Of the 31 recalls from Spacelabs Healthcare, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (6%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–31 of 31

  • SevereFDA (Devices)·Z-2707-2014·2014-10-01

    Spacelabs Patient Monitor Recall for Missing Audible Alarms in End Case Mode

    Spacelabs Healthcare is recalling 222 patient monitors because they may fail to provide audible alarms in End Case mode, a defect missed in a previous recall.

    Product
    Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models are 91367, 91369, 91370, 91387, and 91393 are sold with Perioperative Mode (option D), which includes Start case/End case functionality, Upgrade Kit 040-1548-00.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2586-2014·2014-09-10

    Spacelabs Ariatele Telemetry Transmitter Recalled for SpO2 Display Errors

    Spacelabs is recalling Ariatele Telemetry Transmitters because they may display SpO2 values when sensors are disconnected or failed.

    Product
    ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Physiological patient monitor. Used in a hospital environment.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2077-2014·2014-07-23

    Spacelabs Ultraview SL Multigas Module Recalled for Invalid MAC Display

    Spacelabs Healthcare is recalling 8 Ultraview SL Multigas Modules because the software displays an invalid Minimum Alveolar Concentration value.

    Product
    Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). Provides a means of monitoring a variety of gas concentrations and alert clinical personnel when the concentration of anesthetic agent(s), oxygen, carbon dioxide or nitrous oxide moves outside
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1852-2014·2014-07-02

    Spacelabs Qube Compact Monitor Recalled for Network Connection Loss

    Spacelabs Healthcare is recalling Qube Compact Monitors due to a potential loss of network connection when switching to the Qube Docking Station without powering down.

    Product
    Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are reported by Spacelabs Healthcare parameter modules and/or other physiologic monitors via Flexport interfaces.
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1824-2014·2014-06-25

    Spacelabs Ventilator Interface Recalled for Minute Volume Display Error

    Spacelabs Healthcare is voluntarily recalling Ventilator Flexport Interfaces because the bedside monitor may display minute volume values up to ten times the actual value.

    Product
    Spacelabs Healthcare Ventilator Flexport Interface, Model 90436A-07
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2014·2014-06-11

    Spacelabs Ultraview SL Command Module Recalled for Software Anomaly

    Spacelabs Healthcare is recalling 64 Ultraview SL Command Modules because a software anomaly causes false positive temperature alarms.

    Product
    Spacelabs 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 acquire, monitor, and process various clinical parameters from a patient in a clinical environment.
    Category
    Medical Device
    Distribution
    1 state

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Spacelabs Healthcare

American medical equipment manufacturer

Country
United States
Founded
1958
Parent company
OSI Systems

Official website

Source: Wikidata (Q7572694), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.