BEUDAMED
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    STEVE MADDEN

    FDA UDI
    FGX INTERNATIONAL INC.·00193033283417·

    Gobble

    FDA UDI
    Germiphene Corporation·00850046436307·Gobble Plus - Evacuation System Cleaner - 2 Ltr

    Gobble

    FDA UDI
    Germiphene Corporation·00850046436314·Gobble Plus - Evacuation System Cleaner - 10 Ltr

    RENASYS GO NPWT DEVICE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MEDICAL LTD.·Product code OMP·May 19, 2017

    SYNCROMED EL

    FDA Adverse Event
    Other ·RICE CREEK MANUFACTURING·Product code LKK·December 22, 2005

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 9, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 22, 2012

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·April 21, 2020

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·August 21, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 26, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·February 23, 2018

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 23, 2014

    INTEGRATED APD SET W/CASSETTE3 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 14, 2011

    METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·March 29, 2017

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 5, 2017

    ERYTYPE S ABD+REV A1,B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·February 23, 2021

    ERYTYPE S ABD+REV A1,B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·February 23, 2021

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·April 22, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 10, 2012

    1-DAY ACUVUE MOIST

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPL·October 8, 2020