BEUDAMED
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    LIGAFIX INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO THE BOLD SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERMAL CAUTERY FORCEPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    FAST CATH, 11F, 12CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL CENTER·Product code DYB·May 12, 2008

    HUDSON VENTILATOR TUBING SET, LONG LENGTH

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BZO·April 10, 2013

    FLEXIMA BILIARY CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·April 18, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 19, 2008

    RECLAIM DISTAL TAPERED 19X190

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 7, 2014

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015