BEUDAMED
    26 results · 13ms · Sources: EU EUDAMED, US FDA

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    11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021) 11272VHU-TL 11272VHUK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021)

    FDA Recall
    Open, Classified ·Karl Storz Endoscopy·Product code FBO·April 1, 2022

    Remel Haemophilus Test Medium (150 mm) 10/PK, REF 04033 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests with Haemophilus species.

    FDA Recall
    Open, Classified ·Remel Inc·Product code JSO·March 10, 2021

    Remel Haemophilus Test Medium(100mm) 10/PK, REF: R01503 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests with Haemophilus species.

    FDA Recall
    Open, Classified ·Remel Inc·Product code JSO·March 10, 2021

    THERAKOS CELLEX Photopheresis Procedural Kit, CLXUSA

    FDA Recall
    Open, Classified ·Mallinckrodt Pharmaceuticals Ireland Ltd College Business & Technology Park Blanchardstown Road North Dublin·Product code LNR·December 10, 2021

    VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.

    FDA Recall
    Open, Classified ·Ortho-Clinical Diagnostics, Inc.·Product code JRC·December 10, 2021

    Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product Number/CFN: 178083, 178093, 178094

    FDA Recall
    Open, Classified ·Product code GEI·March 5, 2021

    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.

    FDA Recall
    Open, Classified ·Medical Components, Inc dba MedComp·Product code LJT·January 13, 2021

    Monaco RTP System, Software Builds 5.40.00, 5.40.01, 5.40.02, and 5.51.10

    FDA Recall
    Open, Classified ·Elekta Inc·Product code MUJ·July 26, 2021

    Tenaculum, Plastic

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    IUD Insertion Pack

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    Foundation Kit

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    Cardiosave Hybrid. Intra-Aortic Balloon Pump system.

    FDA Recall
    Open, Classified ·Datascope Corp.·Product code DSP·November 4, 2025

    Cardiosave Rescue. Intra-Aortic Balloon Pump system.

    FDA Recall
    Open, Classified ·Datascope Corp.·Product code DSP·November 4, 2025

    Standard IUD Insertion Kit

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    IUD Insertion Kit

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    Endometrial Biopsy Kit

    FDA Recall
    Open, Classified ·Stradis Medical, LLC dba Stradis Healthcare·Product code HDC·September 10, 2021

    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2). (Different brand names of same product.)

    FDA Recall
    Open, Classified ·Inpeco S.A. Via San Gottardo 10 Lugano Switzerland·Product code CEM·September 10, 2021

    TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)

    FDA Recall
    Open, Classified ·Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy·Product code JDC·January 25, 2023

    REF 8L92-22, Abbott Activated Alanine aminotransferase, for use with Architect, IVD, CE, UDI: (01) 00380740161859

    FDA Recall
    Open, Classified ·Abbott Laboratories·Product code CKA·June 10, 2021

    REF 8L92-42, Abbott Activated Alanine Aminotransferase, for use with Architect, IVD, CE, UDI: (01) 00380740161866

    FDA Recall
    Open, Classified ·Abbott Laboratories·Product code CKA·June 10, 2021