BEUDAMED
    41 results · 63ms · Sources: EU EUDAMED, US FDA

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    WALGREENS

    FDA Adverse Event
    Injury ·QIDONG FARJOY MEDICAL MATERIAL CO LTD·Product code KGX·May 3, 2023

    SOFTHEAT

    FDA Adverse Event
    Injury ·KAZ USA, INC.·Product code IRT·June 22, 2015

    Alere Blood Collection Kit (Consumer Life Insurance), Product K6700, each kit packed in a bag or envelope and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions. Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011

    OPTIFLUX

    FDA Adverse Event
    Injury ·FRESENIUS USA MANUFACTURING INC.·Product code KDI·February 24, 2025

    Appraise A1C Test Pak Kit (Consumers Life Insurance Company), Product K7100, each kit packed in a bag or envelope and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions. Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011

    PHILIPS SONICARE

    FDA Adverse Event
    Other ·PHILIPS ORAL HEALTHCARE·Product code JES·May 31, 2012

    SOFTHEAT

    FDA Adverse Event
    Injury ·KAZ USA, INC.·Product code IRT·October 7, 2015

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code QFG·January 24, 2022

    PULSE GEN MODEL 104

    FDA Adverse Event
    Malfunction ·CYBERONICS·Product code LYJ·September 12, 2016

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION - RENAL DIVISION·Product code KDJ·January 31, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·May 20, 2011

    PULSE GEN MODEL 105

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·August 15, 2018

    CURE PRODUCTS

    FDA Adverse Event
    Injury ·CONVATEC·Product code EZD·November 29, 2023

    CURE PRODUCTS

    FDA Adverse Event
    Injury ·CONVATEC·Product code EZD·November 29, 2023

    TMETRIX PR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·November 17, 2017

    PULSE GEN MODEL 106

    FDA Adverse Event
    Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·September 20, 2019

    PULSE GEN MODEL 106

    FDA Adverse Event
    Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·January 13, 2020

    SOFTHEAT

    FDA Adverse Event
    Other ·KAZ USA, INC.·Product code IRT·March 16, 2015

    PULSE GEN MODEL 106

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·April 10, 2019

    PULSE GEN MODEL 106

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·November 30, 2018