BEUDAMED
    17 results · 33ms · Sources: EU EUDAMED, US FDA

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    ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code HWT·June 29, 2022

    EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD) Part Number: CUI8070S

    FDA Recall
    Open, Classified ·DePuy Spine, Inc.·Product code MAX·May 20, 2022

    EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD). Part Number: CUI8060L

    FDA Recall
    Open, Classified ·DePuy Spine, Inc.·Product code MAX·May 20, 2022

    Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code OIY·February 15, 2023

    Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code KRO·February 15, 2023

    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code KRO·February 15, 2023

    Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code KRO·February 15, 2023

    ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code MBH·March 12, 2024

    MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000, 136356000, 136358000, 136360000

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code LZY·May 18, 2022

    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code KRO·February 15, 2023

    DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212723

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code MAI·April 13, 2023

    DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212722

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code MAI·April 13, 2023

    DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212725

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code MAI·April 13, 2023

    COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code LXH·February 24, 2025

    COR Disposable Kit, 8 mm. Cartilage Transplant System.

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code LXH·February 24, 2025

    DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212724

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code MAI·April 13, 2023

    DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212726

    FDA Recall
    Open, Classified ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code MAI·April 13, 2023