BEUDAMED
    296 results · 25ms · Sources: EU EUDAMED, US FDA

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    Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM, LAG SCR 12.7D X 55 MM SHO up to 100MM, LAG SCR 12.7D X 55MM STAN up to 155 MM, LAG SCR 15.8D X 55MM LARG up to 155 MM

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code JDO·October 11, 2013

    THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105 14-451110 14-451115 14-451120 14-451125 14-451130 . The product is a metallic bone fixation system.

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code JDO·January 7, 2020

    HipLOC Hip Fracture Fixation System-Hiploc System 135 Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures

    FDA Recall
    Terminated ·Biomet UK Ltd. Waterton Industrial Estate Bridgend United Kingdom·Product code JDO·August 9, 2018

    HipLOC Hip Fracture Fixation System- Hiploc System 130 Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-130-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures

    FDA Recall
    Terminated ·Biomet UK Ltd. Waterton Industrial Estate Bridgend United Kingdom·Product code JDO·August 9, 2018

    HipLOC Hip Fracture Fixation System-Hiploc System 135 Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures

    FDA Recall
    Terminated ·Biomet UK Ltd. Waterton Industrial Estate Bridgend United Kingdom·Product code JDO·August 9, 2018

    TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The Biomet Hip Fracture Plating Systems are indicated for use in the open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures and intertrochanteric fractures. Fracture plates with six or more femoral shaft fixation screw holes are also indicated for subtrochanteric fractures as well as proximal femoral osteotomies

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDO·June 10, 2016

    HipLOC Hip Fracture Fixation System-Hiploc System 140 Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-140-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures

    FDA Recall
    Terminated ·Biomet UK Ltd. Waterton Industrial Estate Bridgend United Kingdom·Product code JDO·August 9, 2018

    Custom Made Implant System with Minimum Invasive Grower (MIG) component

    FDA Recall
    Terminated ·Howmedica Osteonics Corp.·Product code JDO·December 21, 2017

    ViewRay System: Model No. 10000 and 20000 for radiation treatment. PN11440 MRIdian System Treatment Planning and Delivery System (TPDS) software

    FDA Recall
    Terminated ·Viewray, Inc.·Product code IYE·November 18, 2019

    Centricity Enterprise Web

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Universal Viewer Zero Footprint Client

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Radiology RA600

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Cardiology CA1000

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity PACS RA1000

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Fisher Wallace Stimulator Models FW-100 and FW-200

    FDA Recall
    Open, Classified ·Fisher Wallace Laboratories Inc.·Product code QJQ·April 6, 2023

    SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic diagnostic imaging device.

    FDA Recall
    Terminated ·Heidelberg Engineering GmbH Tiergartenstr. 15 Heidelberg Germany·Product code OBO·July 3, 2019

    Ventana HE 600 System, automated slide preparer, for use in laboratories.

    FDA Recall
    Open, Classified ·Ventana Medical Systems Inc·Product code KPA·June 1, 2022

    BIOCARE Medical , IntelliPath FLX, Automated Staining Instrument, Ref: " Model Number:IPS0001US and IPS0001INTL containing software version 3.5.3.1

    FDA Recall
    Terminated ·Biocare Medical, LLC·Product code KPA·February 25, 2021

    REF 800-05-035, ENZTEC FEMORAL IMPACTOR - DJO, (01) 09421028110624 (10) 999999, To be used only with DJO EMPOWR 3D KNEE

    FDA Recall
    Terminated ·Enztec Limited 26 Dakota Crescent, Sockburn Christchurch New Zealand·Product code HWA·August 16, 2019

    Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following DJO, LLC / DJO FRANCE kits:

    FDA Recall
    Open, Classified ·DJO, LLC·Product code ITX·September 7, 2021