BEUDAMED
    36 results · 18ms · Sources: EU EUDAMED, US FDA

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    Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)

    FDA Recall
    Open, Classified ·International Life Sciences·Product code OWW·February 6, 2026

    LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 .

    FDA Recall
    Open, Classified ·Zest Anchors LLC·Product code DZE·November 22, 2019

    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

    Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

    FDA Recall
    Open, Classified ·Wright Medical Technology Inc·Product code HRS·December 3, 2021

    UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

    FDA Recall
    Open, Classified ·Neotract Inc·Product code PEW·June 24, 2022

    remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

    FDA Recall
    Open, Classified ·Remel, Inc·Product code JSI·February 13, 2025

    Tacy Medical, Inc PORT ACCESS TRAY, Sterile, QTY 20. Manufactured for Tracy Medical, Inc.

    FDA Recall
    Open, Classified ·Stradis Healthcare·Product code LRS·December 15, 2022

    remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

    FDA Recall
    Open, Classified ·Remel, Inc·Product code JSI·February 13, 2025

    LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25). Product Code: SET-0021-25.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FRN·June 24, 2025

    Vital Care Products NEONATAL PICC TRAY, Sterile, QTY 20. Manufactured for Vital Care Products, Inc.

    FDA Recall
    Open, Classified ·Stradis Healthcare·Product code OWL·December 15, 2022

    REF: 126590, MEDLINE, STERILE ULTRASOUND GEL, 0.70 FL oz. (20 mL), QTY: 50, STERILER, CE 2292

    FDA Recall
    Open, Classified ·Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S. Akcaburgaz Mahallesi Muhsin Yazicioglu Caddesi No:45/5 Esenyurt Turkey·Product code MUI·June 9, 2023

    REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile

    FDA Recall
    Open, Classified ·Osteomed, LLC·Product code GWO·May 31, 2023

    Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

    FDA Recall
    Open, Classified ·Medical Action Industries, Inc.·Product code LRO·March 17, 2026

    Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve

    FDA Recall
    Open, Classified ·Percussionaire Corporation·Product code BZO·August 21, 2024

    Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve

    FDA Recall
    Open, Classified ·Percussionaire Corporation·Product code BZO·August 21, 2024

    LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FRN·June 24, 2025

    LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FRN·June 24, 2025

    LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Product Code: SET-0032-25.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FRN·June 24, 2025

    LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25), Product Code: SET-0013-25. for intravenous infusion.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FPA·August 1, 2024

    IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump Administration Set.

    FDA Recall
    Open, Classified ·Fresenius Kabi USA, LLC·Product code FRN·November 3, 2025