BEUDAMED
    551 results · 13ms · Sources: EU EUDAMED, US FDA

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    Olympus Pleuravideoscope, Model LTF-160

    FDA Recall
    Terminated ·Olympus Corporation of the Americas·Product code GCJ·March 23, 2020

    Olympus Pleuravideoscope, Model LTF-240

    FDA Recall
    Terminated ·Olympus Corporation of the Americas·Product code GCJ·March 23, 2020

    CERTAIN BELLATEK TITANIUM ABUTMENT 5.0MM Reference Number: IEDAT5

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    CERTAIN BELLATEK TIN ABUTMENT 5.0MM Reference Number: IEDAN5

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Reference Numbers: 3DPMSER, 3DPMSERQ

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    CERTAIN BELLATEK TIN ABUTMENT 4.1MM Reference Number: IEDAN4

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    CERTAIN BELLATEK TITANIUM ABUTMENT 6.0MM Reference Number: IEDAT6

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    CERTAIN BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: IEDAT4

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: EDAT4

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NHA·August 31, 2020

    Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·December 6, 2019

    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (23mm) 9630TF23 UDI:00690103201246

    FDA Recall
    Terminated ·Edwards Lifesciences, LLC·Product code NPT·July 9, 2019

    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (26mm) 9630TF26 UDI:00690103201253

    FDA Recall
    Terminated ·Edwards Lifesciences, LLC·Product code NPT·July 9, 2019

    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (29mm) 9630TF29 UDI:00690103201260

    FDA Recall
    Terminated ·Edwards Lifesciences, LLC·Product code NPT·July 9, 2019

    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (20 mm) 9630TF20 UDI:00690103201239

    FDA Recall
    Terminated ·Edwards Lifesciences, LLC·Product code NPT·July 9, 2019

    i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI: 00054749001255)

    FDA Recall
    Terminated ·Abbott Point Of Care Inc.·Product code JQP·September 12, 2017

    Disposable Humidification Flask, Reference Part Number K-MINC-CTS-S, Order Number G32707

    FDA Recall
    Terminated ·Cook Medical Llc·Product code MQG·December 16, 2020

    Blood Glucose Monitoring System, Model Number 08453071001 ACCU-CHEK GUIDE RETAIL KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. The Accu-Chek Guide blood Glucose Monitoring System is intended for in vitro diagnostic single-patient use by people with diabetes. The Accu-Chek Guide Blood Glucose Monitoring System is intended to be used by a single person and should not be shared.

    FDA Recall
    Terminated ·Roche Diabetes Care, Inc.·Product code NBW·September 30, 2019

    Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. The Accu-Chek Guide blood Glucose Monitoring System is intended for in vitro diagnostic single-patient use by people with diabetes. The Accu-Chek Guide Blood Glucose Monitoring System is intended to be used by a single person and should not be shared.

    FDA Recall
    Terminated ·Roche Diabetes Care, Inc.·Product code NBW·September 30, 2019

    Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK GUIDE SAMPLE KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. The Accu-Chek Guide blood Glucose Monitoring System is intended for in vitro diagnostic single-patient use by people with diabetes. The Accu-Chek Guide Blood Glucose Monitoring System is intended to be used by a single person and should not be shared.

    FDA Recall
    Terminated ·Roche Diabetes Care, Inc.·Product code NBW·September 30, 2019

    Blood Glucose Monitoring System, Model Number 07400942001 ACCU-CHEK GUIDE METER ONLY MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. The Accu-Chek Guide blood Glucose Monitoring System is intended for in vitro diagnostic single-patient use by people with diabetes. The Accu-Chek Guide Blood Glucose Monitoring System is intended to be used by a single person and should not be shared.

    FDA Recall
    Terminated ·Roche Diabetes Care, Inc.·Product code NBW·September 30, 2019