BEUDAMED
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    M1 CAPNOGRAPHY MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    K133801

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 31, 2024

    KIMGUARD ONE STEP STERILIZATION WRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACE PROXIMAL HUMERAL NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 26, 2021

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 27, 2020

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·October 1, 2014

    AEQUALIS

    FDA Adverse Event
    Injury ·TORNIER SAS·Product code KWS·May 23, 2013

    RESIDENT BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·May 12, 2011

    Zimmer M/DN Intramedullary Fixation 4.2 dia. cortical screw, 3.5 mm hex head, 70 mm length, 22-13-5 stainless steel, sterile bone screw; Cat. no. 2253-70-42 (00225307042).

    FDA Recall
    Terminated ·Zimmer Inc.·Product code NDJ·June 26, 2006