BEUDAMED
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    ROGACHEFSKY DISTAL RADIUS PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981283·anteriors; shade C2; mould BIM4

    Symmetry Surgical®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482087626·Symmetry® Forceps, Tenaculum, Ratcheting Handle...

    MEADOX INTRA-AORTIC GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    READER, INOCULUM, STDIZED.

    FDA 510(k)

    HEARTSTART MRX - EMS DEFIB

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 20, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·February 1, 2011

    The Bigger Better-Bladder, Catalog Number BBB38 (with 3/8 inch ID tubing), Sterile, Single use only --- Manufactured for: Circulatory Technology Inc., 21 Singworth Street, Oyster Bay, 11771 (516) 624-2424 --- 510 (k) 981284.

    FDA Recall
    Terminated ·Circulatory Technology Inc·Product code DTN·June 3, 2009