BEUDAMED
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    BARD LATEX URINARY CATHETERS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BARDIA FOLEY CATHETER SILICONE COATED K922431

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·November 1, 2021

    HEARTSPAN STEERABLE INTRODUCER KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDRAD TRANSFER SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·December 13, 2010

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·February 6, 2014