BEUDAMED
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    MEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·November 7, 2013

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NEK·December 18, 2012

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code NEK·November 28, 2012

    STRYKEFLOW

    FDA Adverse Event
    Other ·STRYKER CORPORATION·Product code GCJ·August 7, 2023

    NUCLEUS 24 CHANNEL COCHLEAR INPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·December 23, 2008

    BAXTER INTERLINK SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·August 11, 1993

    MEW MEDICAL TECHNOLOGY LTD - SAFETY SYRINGE

    FDA Adverse Event
    Malfunction ·NEW MEDICAL TECHNOLOGY, LTD/ NEW MEDICAL HOUSE·Product code FMF·August 12, 2003

    CONFIRM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (CRM-KISTA)·Product code MXC·December 18, 2015

    EXPRT REVISION HIP, LATERAL OFFSET PROXIMAL BODY, 75MM

    FDA Adverse Event
    Injury ·ENCORE MEDICAL L.P·Product code KWZ·January 3, 2024

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 29, 2022

    PRIMARY MICROBORE GEMSTAR SET WITH 0.2MICRON FILTER

    FDA Adverse Event
    Injury ·Product code FPA·December 1, 2011

    OCH OSANA COVID TEST KIT

    FDA Adverse Event
    Malfunction ·OSANG HEATLHCARE/OSANG LLC.·Product code QKP·October 17, 2024

    MENTOR SILICONE GEL BREAST IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 28, 2018

    FLOWFLEX COVID-19 ANTIGEN HOME TEST

    FDA Adverse Event
    Malfunction ·ACON LABORATORIES, INC.·Product code QKP·February 16, 2023

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·November 4, 2013

    CPAP MACHINE

    FDA Adverse Event
    Injury ·PHILIPS/RESPIRONICS, INC.·Product code BZD·February 25, 2022

    DEES DEESS GP586 PERMANENT HAIR REMOVAL DEVICE, 350,000 FLASHES HOME USE, IPL HA

    FDA Adverse Event
    Injury ·SHENZHEN GSD TECH CO., LTD·Product code OHT·July 29, 2019

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·June 7, 2022

    530G INSULIN PUMP MMT-751LNAB

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·March 16, 2019

    RHOPHYLAC

    FDA Adverse Event
    Malfunction ·CSL BEHRING·Product code FMF·November 18, 2010