BEUDAMED
    41 results · 14ms · Sources: EU EUDAMED, US FDA

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

    MONARCH Bronchoscope. Model Number: MBR-000211-B

    FDA Recall
    Open, Classified ·Auris Health, Inc·Product code QNW·October 18, 2025

    MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery

    FDA Recall
    Open, Classified ·Megadyne Medical Products, Inc.·Product code GEI·June 1, 2023

    STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening, loosening, or removing of screw implants during orthopaedic surgery. Part Number: 03.130.010

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HXX·April 25, 2024

    MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB, MON-000008 with software

    FDA Recall
    Open, Classified ·Auris Health, Inc·Product code EOQ·January 21, 2026

    TFNA Femoral Nail 9mm, right, 130, L 235mm-Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.944S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HSB·January 24, 2024

    VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HRS·January 24, 2024

    Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code JDR·August 30, 2022

    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

    Opal, Intervertebral Cage, 10x32mm, h 11mm, Revolvable-Indicated for degenerative spine disease Part Number: 08.803.231S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code N/A·January 24, 2024

    13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX, sterile -Intended to facilitate tibiotalocalcaneal arthrodesis to treat severe foot/ankle deformity, arthritis, instability, and skeletal defects after tumor resection. Part Number: 04.008.378S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HSB·January 24, 2024

    2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical, orthopedic, pneumatic powered & accessory/attachment Product Code: 310.25S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HSZ·January 24, 2024

    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

    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