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    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·November 20, 2025

    REBAR CATHETER

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·December 6, 2024

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·June 23, 2025

    SPINAL 22G WHITACRE FORTEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD INC.·Product code CAZ·March 17, 2016

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·May 4, 2025

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·April 9, 2025

    EMBOTRAP III 5 MM X 37 MM

    FDA Adverse Event
    Injury ·NEURAVI LTD.·Product code NRY·August 4, 2021

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Death ·HEARTWARE, INC.·Product code DSQ·March 12, 2021

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 26, 2018

    AXIUM PRIME BRPL HLX

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code KRD·April 21, 2025

    AXIUM PRIME BRPL 3D

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code KRD·November 29, 2018

    VITEK® 2 YEAST (YST) IDENTIFICATION (ID) TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code JXB·February 7, 2017

    REMEL SABOURAUD DEXTROSE CONTACT PLATE

    FDA Adverse Event
    Malfunction ·REMEL THERMO FISHER SCIENTIFIC·Product code JSG·August 7, 2017