BEUDAMED
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    PERCEVAL SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP.·Product code LWR·July 24, 2019

    STENT

    FDA Adverse Event
    Injury ·UNK·Product code MAF·December 14, 2023

    2.7 DEGREE ANGLED SAGITAL SAW

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·April 4, 2019

    IMO-402 Mononucleosis Rapid Test Device (Whole Blood/Serum/Plasma). Catalog #IMO-402/94201 The MONO test (Whole Blood) is a rapid chromatographic immunoassay for the qualitative detection of Infectious Mononucleosis heterophile antibodies in whole blood to aid in the diagnosis of infectious Mononucleosis.

    FDA Enforcement
    Class III ·Terminated·Alere San Diego, Inc.·April 24, 2013

    IMO SANITARY NAPKINS

    FDA Adverse Event
    Injury ·CHUNG-A BEAUTY & HEALTH CO.,LTD.·Product code HHD·February 3, 2023

    IMO-402 Mononucleosis Rapid Test Device (Whole Blood/Serum/Plasma). Catalog #IMO-402/94201 The MONO test (Whole Blood) is a rapid chromatographic immunoassay for the qualitative detection of Infectious Mononucleosis heterophile antibodies in whole blood to aid in the diagnosis of infectious Mononucleosis.

    FDA Recall
    Terminated ·Alere San Diego, Inc.·Product code KTN·February 26, 2013

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 1, 2002

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 6, 2002

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 6, 2002

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·December 19, 2003

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·September 7, 2000

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·September 6, 2002

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·November 29, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·February 28, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 27, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·February 27, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·February 28, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·February 27, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·February 26, 2001

    MIDAS REX I MO

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 1, 2001