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

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    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.

    FDA Recall
    Completed ·Lens.com·Product code LPM·August 14, 2018

    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.

    FDA Recall
    Completed ·Allied Vision Group Inc·Product code LPM·August 1, 2018

    Leccurate SARS-CoV-2, Antigen Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for the qualitative detection of antigen SARS-CoV-2 in clinical samples (nasal swab).

    FDA Recall
    Completed ·LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD Building 7-1 NO. 37 Chaoqian Rd; Changping Tech Zone Beijing China·Product code QKP·April 26, 2021

    Leccurate SARS-CoV-2, Antibody Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for qualitative detection of IgM and/or IgG antibodies to SARS-CoV-2 in human serum, plasma and venipuncture whole blood for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.

    FDA Recall
    Completed ·LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD Building 7-1 NO. 37 Chaoqian Rd; Changping Tech Zone Beijing China·Product code QKO·April 26, 2021

    Illumina NextSeq 550Dx, REF: 20005715, CE, IVD

    FDA Recall
    Completed ·Illumina, Inc.·Product code PFF·February 22, 2022

    Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.

    FDA Recall
    Completed ·RHONDIUM LIMITED·Product code EBF·January 31, 2019

    LINQ II Insertable Cardiac Monitor

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code MXD·January 18, 2022

    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System s intended use environment includes anatomic pathology (AP) laboratories and histology facilities within hospital, clinic, reference, or private lab settings. The System is to be operated by qualified users in

    FDA Recall
    Completed ·Ventana Medical Systems Inc·Product code KPA·October 4, 2019

    Outer Packaging Label: Protekt Sharps Safety Knives - REF: PG 44620MU, Sterile R, Multi-Use 2.2mm Double Bevel Slit, Angled 6 units, Individual Packaging Label: ProTekt Sharps Safety Knives - REF: PG 44620MU,2.2mm double Bevel Slit, Sterile R, Angled 1 unit, Handle Labeling; 2.5mm slit double bevel

    FDA Recall
    Completed ·International Science & Technology, LP, DBA Diamatrix Ltd.·Product code HNN·February 24, 2022

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Recall
    Completed ·Townsend Design·Product code IQI·September 23, 2023

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Recall
    Completed ·Townsend Design·Product code IQI·September 23, 2023

    CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040

    FDA Recall
    Completed ·Townsend Design·Product code IQI·September 23, 2023

    SynCardia 50cc TAH-t, Clinical, REF 570500, Sterile EO

    FDA Recall
    Completed ·SynCardia Systems LLC·Product code LOZ·August 1, 2023

    Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210

    FDA Recall
    Completed ·Philips Ultrasound, Inc.·Product code IYN·October 9, 2023

    Access Vitamin B12 Reagent, Catalog Number 33000, Lot Number 439850

    FDA Recall
    Completed ·Beckman Coulter, Inc.·Product code CDD·February 27, 2025