BEUDAMED
    138 results · 21ms · Sources: EU EUDAMED, US FDA

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    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

    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

    Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary internal fixation and stabilization of osteotomies and fractures, including comminuted fractures, supracondylar fractures, intra-articular and extra-articular condylar fractures, fractures in osteopenic bone, nonunions, and malunions. Item Number: 00235710106

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code HRS·June 27, 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

    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