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    Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006

    FDA Recall
    Open, Classified ·Schiller, Ag Altgasse 68 Baar Switzerland·Product code MHX·August 8, 2025

    Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

    FDA Recall
    Open, Classified ·Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom·Product code LDD·October 28, 2024

    Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model RCSV2 device is a hemodynamics recording computer system that monitors, measures, displays, records and stores various physiologic and blood flow parameters based on the output from one or more electrodes, transducers, or measuring devices. The system is used for documenting and monitoring patients undergoing diagnostic and interventional catheter-based procedures. The procedures can be performed in the clinical areas of invasive cardiology, interventional radiology, and cardiac electrophysiology.

    FDA Recall
    Open, Classified ·Merge Healthcare, Inc.·Product code DQK·August 11, 2025

    Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the Merge Hemo Patient Data Module (PDM). The PDM is a major component of the Merge Hemo system.

    FDA Recall
    Terminated ·Merge Healthcare, Inc.·Product code DQK·March 30, 2015

    CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570

    FDA Recall
    Open, Classified ·Schiller, Ag Altgasse 68 Baar Switzerland·Product code DPS·July 24, 2024