BEUDAMED
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    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·April 1, 2025

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·April 3, 2025

    ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScreen" Drugs of Abuse Test (MET1000/OPI2000)+AMP+BZO+COC+THC", PSD-6MTDBO-300 /"ProScreen" Drugs of Abuse Test (COC/THC)+BZO+MTD+OPI300+OXY", PSCUP-5M-W/ ProScreen" Drugs of Abuse Cup AMP/COC/MET1000/OPI2000/THC), PSD-10MOB "ProScreen" Drugs of Abuse Test (COC/THC)+(MET1000/OPI2000)+(OXY/ MDMA)+AMP+BZO+BUP+MTD", PSD-5M / "ProScreen" Drugs of Abuse Test AMP/COC/MET1000/OPI2000/THC", PSCUPA-10OM / ProScreen" Drugs of Abuse Cup (COC/THC)+(MET1000/OPI2000)+(OXY/ MDMA) +(PCP/AMP)+BAR+BZO

    FDA Recall
    Terminated ·Ameditech Inc·Product code DKC·August 18, 2020

    Toshiba America Medical Systems Angio WorkStation: XIDF-AWS801v6.00, v6.01, and V6.10 System: INFX-8000V Bi-Plane System

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·July 27, 2016

    PERI-STRIPS DRY STAPLE LINE REINFORCEMENT

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·November 24, 2010

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·August 28, 2020

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·August 28, 2020

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·August 27, 2020

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·October 10, 2007

    RADIAL JAW¿ 4

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code KGE·November 2, 2011

    ALARIS SYRINGE MODULE SETS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·January 25, 2018

    ALARIS SYRINGE MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·April 18, 2018

    MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose received by the patient to the targeted area of their body.

    FDA Recall
    Terminated ·Angiodynamics, Inc.·Product code NZT·November 19, 2019

    MICRO-PSD Electron, Catalog Number: PSD-EE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose received by the patient to the targeted area of their body.

    FDA Recall
    Terminated ·Angiodynamics, Inc.·Product code NZT·November 19, 2019

    MICRO-PSD HDR, Catalog Number: PSD-HB5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose received by the patient to the targeted area of their body.

    FDA Recall
    Terminated ·Angiodynamics, Inc.·Product code NZT·November 19, 2019

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·October 7, 2010

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·October 7, 2010

    ELECTROSURGICAL GENERATOR

    FDA Adverse Event
    Injury ·OLYMPUS WINTER AND IBE GMBH·Product code GEI·November 7, 2014

    Ceramill® Zolid

    FDA UDI
    Amann Girrbach AG·E4947615871·

    Ceramill® Zolid

    FDA UDI
    Amann Girrbach AG·E4947615891·