BEUDAMED
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    PULSE GEN MODEL 106

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·February 19, 2021

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825002275·Diagnostic EP Catheter A-Curve (Josephson/YLW) ...

    ON Q

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH, INC.·Product code MEB·July 5, 2017

    FUSION¿ ENT NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 16, 2019

    BD SAFETYGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·February 23, 2023

    MAGELLAN 3ML SFTY COMBO 23X1

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FMF·September 24, 2022

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 30, 2016

    UNKNOWN ENTERAL FEEDING

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code LZH·February 24, 2023

    STEALTHSTATION I7 INTEGRATED NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·October 2, 2017

    D-FLEX CIRCULAR RETRACTOR 40MM ANG 5MM

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code GCJ·May 12, 2014

    PRIMARY PLUM SET, CLAVE SECONDARY PORT, 2 CLAVE Y-SITES, 0.2 MICRON FILTER, SECU

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·May 23, 2024

    SI AVANTI+ 6F STD W/GW NO OBT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·May 31, 2019

    SABER 2MM20CM 150

    FDA Adverse Event
    Malfunction ·CORDIS CASHEL·Product code LIT·May 10, 2018

    SABER 2MM20CM 150

    FDA Adverse Event
    Malfunction ·CORDIS CASHEL·Product code LIT·May 10, 2018

    SABER 2MM20CM 150

    FDA Adverse Event
    Malfunction ·CORDIS CASHEL·Product code LIT·May 8, 2018

    YOUNG DH Dry Heat Indicators, PRESSURE SENSITIVE LABELS with COLOR INDICATOR STRIP, REF 116312 Intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization process.

    FDA Recall
    Open, Classified ·Young Dental Mfg Co I LLC·Product code JOJ·December 29, 2021

    RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.

    FDA Recall
    Completed ·Appliedvr·Product code QRA·February 27, 2023

    Virtual Reality Behavioral Therapy Device For Pain Relief

    FDA classification
    FDA Class 2 ·Virtual Reality Behavioral Therapy Device For Pain Relief

    LABORATOIRE HRA PHARMA

    FDA registration
    LABORATOIRE HRA PHARMA·2 products·🇫🇷 France

    ASIAWORLD BRA CO LTD

    FDA registration
    ASIAWORLD BRA CO LTD·2 products·🇹🇭 Thailand