BEUDAMED
    10,000 results · 11ms · Sources: EU EUDAMED, US FDA

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    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723

    FDA Recall
    Open, Classified ·Product code KDD·February 27, 2026

    Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)

    FDA Recall
    Open, Classified ·SURGIFY MEDICAL OY Otakaari 5 I Espoo Finland·Product code HBE·April 30, 2026

    Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code PHX·May 20, 2026

    Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

    FDA Recall
    Open, Classified ·SURGIFY MEDICAL OY Otakaari 5 I Espoo Finland·Product code HBE·April 30, 2026

    Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

    FDA Recall
    Open, Classified ·SURGIFY MEDICAL OY Otakaari 5 I Espoo Finland·Product code HBE·April 30, 2026

    Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A

    FDA Recall
    Open, Classified ·Product code OES·May 28, 2026

    Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476

    FDA Recall
    Open, Classified ·Zimmer, Inc.·Product code PHX·May 20, 2026

    Ami HTX.

    FDA Recall
    Open, Classified ·Spectral Instruments Inc·Product code RCE·May 13, 2025

    HORIBA custom configured fluorescence instrument, modular Fluorolog-QM

    FDA Recall
    Open, Classified ·Horiba Instruments Incorporated·Product code REM·March 28, 2024

    Virus Counter Platform with Model Name VC3100

    FDA Recall
    Open, Classified ·Sartorius Corporation·Product code REQ·March 11, 2022

    TASE 500 Imaging systems

    FDA Recall
    Open, Classified ·COLLINS AEROSPACE·Product code RET·January 29, 2019

    ClubMax Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

    FDA Recall
    Open, Classified ·IN MY BATHROOM LLC·Product code RHP·January 27, 2022

    Yamaha Surface Mounter YR series, YS series, i-Pulse series, Sigma series, S series, M series. Affected models: YSM10, YSM20R(SV)-1, YSM20R(SV)-2, YSM20R-1, YSM20R-2, YSM20-1, YSM20-2, YSM20W-2, YRM20-1, YRM20-2, SIGMA-G5S2, S20, M20 ***Updated as of 6/10/2024*** Surface Mounter model S10, YC8. Component Dispenser model YSD

    FDA Recall
    Open, Classified ·YAMAHA MOTOR CORPORATION·Product code RGA·April 17, 2024

    NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.

    FDA Recall
    Open, Classified ·Northeast Scientific Inc.·Product code QTF·August 29, 2025

    Fusion Pro 24, Model 17000

    FDA Recall
    Open, Classified ·Epilog Laser Corp.·Product code RHK·August 8, 2024

    SenTiva, REF: 1000C, Generators Part of the VNS Therapy System with Microburst Stimulation. Used for Vagus Nerve Stimulation (VNS).

    FDA Recall
    Open, Classified ·LivaNova USA, Inc.·Product code LYJ·December 12, 2024

    Lazervida 10W diode laser cutter and engraver with Lazervida shield.

    FDA Recall
    Open, Classified ·Flux Technology Inc.·Product code RHK·February 19, 2025

    SlideView VS200 slide viewer,

    FDA Recall
    Open, Classified ·EVIDENT SCIENTIFIC INC·Product code RIB·July 22, 2024

    MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code N/A·April 30, 2020