BEUDAMED
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    Motion Hybrid Wire Guide

    FDA UDI
    HERAEUS MEDICAL COMPONENTS LLC·00827002448469·

    Motion Hybrid Wire Guide

    FDA UDI
    HERAEUS MEDICAL COMPONENTS LLC·00827002448483·

    MUELLER HINTON AGAR W/CHOCOLATE, MH W/CHOC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·20801902115663·Arrowg+ard Blue Plus(R) Three-Lumen CVC Kit

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902115666·Multi-Lumen Central Venous Catheterization Kit ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902062550·Multi-Lumen Central Venous Catheterization Kit ...

    COOK MOTION HYBRID WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DQX·December 10, 2020

    MOTION HYBRID WIRE GUIDE

    FDA Adverse Event
    Malfunction ·HERAEUS MEDICAL COMPONENTS·Product code EZB·March 7, 2022

    MOTION HYBRID WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code EZB·January 20, 2022

    Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1

    FDA Enforcement
    Class II ·Terminated·Arrow International Inc·June 6, 2018

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 11, 2020

    MELODY TRANSCATHETER PULMONARY VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·December 11, 2020

    remel SUPERPACK CS/ 500 SEG/FLASK, REF R01626, Qty:50, plate label: REMEL MH W/OXACILLIN Product Usage: Recommended for the use in qualitative procedures to screen Staphylococcus aureus for resistance to penicillinase- resistance penicillins (e.g., methicillin, nafcillin, and oxacillin).

    FDA Enforcement
    Class II ·Terminated·Thermo Fisher·June 20, 2018

    HEALON

    FDA Adverse Event
    Injury ·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·July 13, 2000

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·April 2, 2026

    Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·April 11, 2018

    remel SUPERPACK CS/ 500 SEG/FLASK, REF R01626, Qty:50, plate label: REMEL MH W/OXACILLIN Product Usage: Recommended for the use in qualitative procedures to screen Staphylococcus aureus for resistance to penicillinase- resistance penicillins (e.g., methicillin, nafcillin, and oxacillin).

    FDA Recall
    Terminated ·Thermo Fisher·Product code JTZ·May 4, 2018

    D-STAT

    FDA Adverse Event
    Malfunction ·VASCULAR SOLUTIONS·Product code MHW·May 18, 2010

    D-STAT FLOWABLE HEMOSTAT

    FDA Adverse Event
    Death ·VASCULAR SOLUTIONS, INC.·Product code MHW·October 1, 2014

    SURGIGRIP LATEX-FREE SIZE F - 4" X 10 METERS

    FDA Adverse Event
    Injury ·DERMA SCIENCES, INC.·Product code MHW·June 11, 2021