BEUDAMED
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    Replacement Backflush Reservoir, Passive Handpiece

    FDA UDI
    KATALYST SURGICAL LLC·00840096208436·Replacement Backflush Reservoir, Passive Handpiece

    Drive

    FDA UDI
    Drive Devilbiss Healthcare·00822383981635·35" Self AdjustMatt w/RR and pump-P/L

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·30801902116032·Pressure Injectable Arrowg+ard Blue Plus(R) Fou...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902062376·Pressure Injectable Quad-Lumen Central Venous C...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902116038·Pressure Injectable Arrowg+ard Blue Plus(R) Fou...

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·March 28, 2023

    FLEXIVA PULSE ID

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·March 24, 2026

    FLEXIVA PULSE ID

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·April 16, 2026

    FLEXIVA PULSE ID

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·February 23, 2026

    MOXY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·February 26, 2026

    LIGHTTRAIL REUSABLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·March 31, 2026

    Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-45854-PSFM and ASK-42854-PRR

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

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·December 14, 2021

    FLEXIVA PULSE ID

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·April 14, 2026

    FLEXIVA PULSE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·April 16, 2026

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·November 7, 2021

    LIGHTTRAIL REUSABLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·February 5, 2026

    EMBLEM MRI S-ICD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·April 11, 2019

    IMPELLA LP 5.0 PUMP

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·May 1, 2019

    ELECTRODES

    FDA Adverse Event
    Injury ·CONVATEC LIMITED·Product code GEI·April 29, 2014