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    VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012

    FDA Recall
    Open, Classified ·Visionsense, Ltd. 20, Ha-Magshimim Petakh Tikva Israel·Product code OWN·October 17, 2022

    VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001

    FDA Recall
    Open, Classified ·Visionsense, Ltd. 20, Ha-Magshimim Petakh Tikva Israel·Product code OWN·October 17, 2022

    VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS) - 785nm Product Number: 175-0012

    FDA Recall
    Open, Classified ·Visionsense, Ltd. 20, Ha-Magshimim Petakh Tikva Israel·Product code OWN·October 17, 2022

    Quest Spectrum 3 Fluorescent Imaging System Model/Catalog Number: ART-SYS-0029, ART-SYS-0030 The Quest Spectrum3 is a fluorescent imaging system used in capturing and viewing fluorescent images for the visual assessment of blood flow for the evaluation of tissue perfusion, and related tissue-transfer circulation in tissue and free flaps used during plastic and reconstructive surgeries.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code OWN·September 24, 2024

    V-Probe, Endocare Cryo V Probe model # Cryo 206V. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.

    FDA Recall
    Terminated ·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008

    V-Probe, Endocare Cryo V Probe, single unit model # CVA2400. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.

    FDA Recall
    Terminated ·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008

    515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    515B Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    515B Pulse Oximeter, RS232, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    French 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    Spanish 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    100-120V Oxypleth - 520A Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    100-120V Oxypleth - 520A Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    Japanese 100-120V Oxypleth - 520A Pulse Oximeter- Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    Spanish 100-120V 2001 Pulse Oximeter WI - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    100-120V 2001 Pulse Oximeter With Mars - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    Span 100-120V 520A - OxyPleth Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    100-120V 515B with RS-232 Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    100-120V 2001 Pulse Oximeter with Mars, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DQA·November 19, 2009

    REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring.

    FDA Recall
    Terminated ·LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC·Product code MUU·August 8, 2017