BEUDAMED
    28 results · 12ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Open, Classified × Clear all

    NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX

    FDA Recall
    Open, Classified ·NOA Medical Industries Inc·Product code IKX·November 5, 2024

    Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007

    FDA Recall
    Open, Classified ·PYRAMES INC·Product code DXN·February 24, 2025

    Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178402

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178414

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.

    FDA Recall
    Open, Classified ·INCIPIO DEVICES avenue des Paquiers 16 St-Blaise Switzerland·Product code HWA·October 30, 2024

    Compress Device Short Anchor Plug, 10 MM-Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement Item Number: 178552

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1, R560BCS1. Used in cardiopulmonary bypass (CPB) procedures.

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWA·March 3, 2021

    Compress Device Short Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178560

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178412

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178562

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Short Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178564

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178410

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Segmental Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178404

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178565

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178566

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178408

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178568

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023

    Exactech Ergo Impactor Handle, Catalog #321-09-05.

    FDA Recall
    Open, Classified ·Exactech, Inc.·Product code HWA·June 5, 2023

    DJO Surgical: CLP Hip, Stem, Polished Neck, Lateral Offset Implant, Size#3, REF: 426-11-030

    FDA Recall
    Open, Classified ·Product code KWA·August 4, 2023

    Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178556

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KWA·October 9, 2023