BEUDAMED
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    WITHINGS BPM CONNECT BLOOD PRESSURE MONITOR

    FDA Adverse Event
    Injury ·WITHINGS·Product code DXN·July 3, 2023

    BODY SCAN (BIOMETRIC SCALE)

    FDA Adverse Event
    Malfunction ·WITHINGS·Product code FRI·March 12, 2024

    WITHINGS BPM CONNECT

    FDA Adverse Event
    Malfunction ·WITHINGS·Product code DXN·January 20, 2023

    WPM05 - WITHINGS BPM CONNECT

    FDA Adverse Event
    Malfunction ·WITHINGS·Product code DXN·December 13, 2023

    WITHINGS PULSEHR (NEW)

    FDA Adverse Event
    Injury ·WITHINGS S.A.·Product code DQA·December 29, 2021

    PULSE HR

    FDA Adverse Event
    Malfunction ·WITHINGS, INC.·Product code DXH·June 9, 2020

    BP CONNECT

    FDA Adverse Event
    Malfunction ·WITHINGS S.A.·Product code DXN·July 12, 2021

    BLOOD PRESSURE MONITOR CONNECT

    FDA Adverse Event
    Malfunction ·WITHINGS S.A.·Product code DXN·November 17, 2022

    WITHINGS - BPW CONNECT AUTOMATIC BLOOD PRESSURE MONITOR - WHITE/GRAY

    FDA Adverse Event
    Malfunction ·WITHINGS S. A.·Product code DXN·January 8, 2020

    DIMENSION EXL WITH LM

    FDA Adverse Event
    Malfunction ·DIMENSION EXL WITH LM·Product code JJE·August 30, 2018

    NASAL DILATOR

    FDA Adverse Event
    Injury ·"BREATHE WITH EEZ" CORPORATION·Product code LWF·August 25, 1992

    PALMAZ-SCHATZ BALLOON-EXPANDABLE

    FDA Adverse Event
    Injury ·CORONARY STEM WITH DELIVERY SYSTEM·Product code MAF·September 26, 1996

    APOGEE POLYPYRIDINE MESH

    FDA Adverse Event
    TM SYSTEMS WITH INTEL PRO·Product code FTL·May 24, 2007

    UNIVERSAL VENTILATOR CIRCUIT WITH NEBULIZER

    FDA Adverse Event
    Injury ·PROFESSIONAL MEDICAL CIRCUIT WITH NEBULIZER·Product code BZO·January 31, 1997

    PANORAMA CENTRAL STATION WITH TELEPACK

    FDA Adverse Event
    Malfunction ·PANORAMA CENTRAL STATION WITH TELEPACK·Product code MHX·July 31, 2013

    ISPAN PERFLUOROPROPANE (C3F8) GAS

    FDA Adverse Event
    Malfunction ·ALCON - FORT WITH / ALCON LABORATORIES, INC.·Product code LPO·March 26, 2014

    RENU WITH MOISTURE LOC

    FDA Adverse Event
    Injury ·BAUSCH AND LOMB WITH MOISTURE LOC·Product code LPN·June 25, 2006

    CONTROL SYRINGE

    FDA Adverse Event
    Malfunction ·SHERWOOD MEDICAL/MONOJECT MERGED WITH KENDALL·Product code FMF·January 4, 1999

    HILL-ROM BED

    FDA Adverse Event
    Malfunction ·MEPCO/ELECTRA CAPACITOR AS USED WITH HILL-ROM MOTOR·Product code FNL·July 26, 2000

    PFC*SIGMA C/S NPOR FEM RT SZ 4

    FDA Adverse Event
    Injury ·THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT R·Product code JWH·August 7, 2013