BEUDAMED
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    Insulin Pen Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD BBL™ Mueller Hinton Agar with 5% Sheep Blood

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902211768·BD BBL™ Mueller Hinton Agar with 5% Sheep Blood...

    STGC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMPUMEDICS SOMTE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STINGRAY LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·March 26, 2025

    STINGRAY LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·February 3, 2025

    PLATE MUELLER HINTON 5% SB 90MM 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JTZ·March 4, 2021

    BD BBL¿ MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·May 18, 2023

    PLATE MUELLER HINTON AGAR 5% SB 20 EA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·March 23, 2021

    STINGRAY? LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·May 29, 2026

    BBL - MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JTZ·November 1, 2021

    FLEXICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·August 24, 2011

    INGENIO

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·November 3, 2014

    OLYMPUS EVIS EXERA XENON COLONOVIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDF·July 3, 2013

    PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, POROUS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBL·October 17, 2025

    PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025

    PLATE MUELLER HINTON AGAR 5% SB 20 EA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·June 16, 2023

    Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012