BEUDAMED
    41 results · 22ms · Sources: EU EUDAMED, US FDA

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    Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. Item Number: VPX4000 (7273)

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code GEI·September 17, 2024

    Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm Model/Catalog Number: 70-1047-COM0117

    FDA Recall
    Open, Classified ·Prismatik Dentalcraft, Inc.·Product code NHA·September 30, 2025

    Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code LZO·November 2, 2023

    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

    Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code MBI·September 9, 2025

    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

    G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code LPH·February 6, 2023

    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

    (1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item Number: 183108 (4) Vanguard Knee System PS Open Box Femoral; Right; 67.5 mm Item Number: 183110 (5) Vanguard Knee System PS Open Box Femoral; Right; 70 mm Item Number: 183112

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code JWH·December 29, 2022

    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

    JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code KDD·October 21, 2024

    RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code JDI·May 17, 2024

    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