BEUDAMED
    6 results · 12ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Open, Classified × Clear all

    CAPIOX FX25 Hollow Fiber Oxygenator, Catalog Numbers 3CX*FX25REC, 3CX*FX25RWC

    FDA Recall
    Open, Classified ·Terumo Cardiovascular Systems Corporation·Product code DTZ·March 1, 2023

    CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE

    FDA Recall
    Open, Classified ·Terumo Cardiovascular Systems Corporation·Product code DTZ·March 1, 2023

    CAPIOX RX15 Hollow Fiber Oxygenator, Catalog Number 3CX*RX15RE30

    FDA Recall
    Open, Classified ·Terumo Cardiovascular Systems Corporation·Product code DTZ·March 1, 2023

    Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

    FDA Recall
    Open, Classified ·FX SHOULDER·Product code PHX·August 8, 2023

    Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840

    FDA Recall
    Open, Classified ·Western/Scott Fetzer Company·Product code ECX·October 16, 2021

    Medline procedural kits labeled as: 1) BABY CARE KIT UNIV, Pack Number DYKL1025; 2) BABY CARE KIT UNIV, Pack Number DYKL1025H

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code CCX·April 8, 2024