BEUDAMED
    165 results · 24ms · Sources: EU EUDAMED, US FDA

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    BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code MBI·September 23, 2025

    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

    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LZO·March 24, 2025

    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LZO·March 24, 2025

    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LZO·March 24, 2025

    Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LPH·September 26, 2025

    Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size G, Bearing, Model/Catalog Number: 110031013; semi constrained hip prosthesis

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LPH·September 26, 2025

    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LZO·March 24, 2025

    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code LZO·March 24, 2025

    BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045150

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023

    BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023

    BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number:110045154

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code MBI·May 4, 2023

    BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045160

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code MBI·May 4, 2023

    Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023

    Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045157

    FDA Recall
    Open, Classified ·T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel·Product code LXH·May 4, 2023

    Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, Part Number: 1067716

    FDA Recall
    Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

    Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number: 1067718

    FDA Recall
    Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

    3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

    FDA Recall
    Open, Classified ·Zimmer Surgical Inc·Product code FZW·January 2, 2024

    OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602

    FDA Recall
    Open, Classified ·Biomet, Inc.·Product code HSB·November 29, 2022

    ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments holders or tool guides to be used by trained surgeons to guide standard surgical instruments during brain and spine surgeries.

    FDA Recall
    Open, Classified ·MEDTECH SAS 900 Rue Du Mas De Verchant Montpellier France·Product code HAW·September 22, 2021