BEUDAMED
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    COMPRESSOR MINI

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BTI·August 30, 2018

    COMPRESSOR MINI

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BTI·October 12, 2018

    UNK HYLAMER LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·October 29, 1999

    ALWAYS MAXI PAD WITH FLEXI-WINGS, OVERNIGHT EXTRA HEAVY (NOT

    FDA Adverse Event
    Injury ·KNH ENTERPRISE CO. LTD·Product code HHD·October 30, 2009

    BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·August 25, 2020

    THE KOH COLPOTOMIZER SYSTEM

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL - THE KOH COLPOTOMIZER SYSTEM·Product code HEW·February 7, 2011

    BARD RECONIX

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·February 4, 2014

    TORNIER HRS PTC DISTAL STEM DIA 11

    FDA Adverse Event
    Injury ·TORNIER INC·Product code KWS·December 22, 2023

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 21, 2022

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 17, 2022

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 17, 2022

    TOTAL ASR ACET IMP SIZE 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 3, 2015

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 26, 2024

    POWERED 60 ECHELON +, 440MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 22, 2024

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 29, 2022

    PWRD ECH FLEX 45MM 28CM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 10, 2024

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 15, 2012

    SYNERGY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·July 24, 2019

    HANDY SOLUTIONS

    FDA Adverse Event
    Injury ·NINGBO UNICO PRODUCTS CO., LTD FLOOR.3TH, BUILDING·Product code IRT·February 4, 2026

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 19, 2022