BEUDAMED
    2,389 results · 22ms · Sources: EU EUDAMED, US FDA

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    MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515) and 3.5oz tube (Model Number 31535)

    FDA Recall
    Open, Classified ·Integra LifeSciences Corp.·Product code FRO·September 13, 2024

    Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23

    FDA Recall
    Open, Classified ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code GCJ·December 11, 2025

    Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code GAD·May 25, 2023

    Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code GAD·May 25, 2023

    Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code KAL·May 25, 2023

    Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.

    FDA Recall
    Open, Classified ·I.T.S. GmbH Autal 28 Lasnitzhohe Austria·Product code HRS·May 9, 2019

    Epix Universal Clip Applier, REF: CA500, STERILEEO

    FDA Recall
    Open, Classified ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code MDM·January 30, 2024

    Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C

    FDA Recall
    Open, Classified ·Kico Knee Innovation Company·Product code OLO·April 23, 2026

    Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E

    FDA Recall
    Open, Classified ·Kico Knee Innovation Company·Product code OLO·April 23, 2026

    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

    Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CMS Product Description: MFM-CMS is a central monitoring system product, which can connect and manage information from EDAN medical devices. MFM-CMS offers central management for monitoring information from the medical devices. All these collected information can be displayed, printed, alarmed and recorded. Component: No

    FDA Recall
    Open, Classified ·Edan Diagnostics·Product code MHX·October 24, 2025

    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 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

    Streamline OCT Navigated Instruments, Catalog numbers 26-DRILL-MDN 26-FTAP-30-MDN 26-FTAP-35-MDN 26-FTAP-40-MDN 26-FTAP-40-MDN 26-FTAP-45-MDN 26-S-FINDER-MDN Components of a surgical navigation device.

    FDA Recall
    Open, Classified ·RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)·Product code OLO·September 24, 2020

    Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovasculature.

    FDA Recall
    Open, Classified ·Product code QJP·March 8, 2024

    Route 92 Medical, 070 Access System, REF 1004, Rxonly , Sterile EO. Used for introduction of interventional devices into the neurovasculature.

    FDA Recall
    Open, Classified ·Product code QJP·March 8, 2024