BEUDAMED
    23 results · 42ms · Sources: EU EUDAMED, US FDA

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    OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NVP·March 16, 2021

    DEXCOM G6 SENSOR 3 PACK Item Number: 5447552

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code QBJ·March 16, 2021

    Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code FMK·March 16, 2021

    Kangaroo Joey Safety Screw Spike with Flush Bag, Anti-free Flow,1000 mL, Product Code 765100

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NBW·March 16, 2021

    Kangaroo Joey Safety Screw Spike Set, Anti-free Flow, Product Code 765559

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    VAPORIZER VICKS 1.5GAL Item Number: 2354942

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code KFZ·March 16, 2021

    FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code QLG·March 16, 2021

    Kangaroo 924 Safety Screw Spike Set, Product Code 775759

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NVP·March 16, 2021

    Kangaroo Epump Safety Screw Spike Set, Anti-free Flow, Product Code 775659

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code FMK·March 16, 2021

    FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code PZE·March 16, 2021

    ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NBW·March 16, 2021

    FREESTYLE LANCETS 28G 100CT Item Number:2975670

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code FMK·March 16, 2021

    ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NBW·March 16, 2021

    Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a flexible, self-expanding endoluminal stent to the carotid vasculature via over-the-wire (OTW) 5.5F or 6F sheathed delivery systems. The stent is cut from a solid nitinol tube into a fine mesh ( Z configuration) design. The delivery systems consist mainly of an inner shaft and an outer sheath with radiopaque markers, and a Tuohy Borst valve. The inner shaft terminates distally in a catheter tip and originates proximally in a luer hub designed to accept a 0.018 guidewire. The delivery systems have a nominal working length of 135 cm. The self-expanding PRECISE stent is constrained within the space between the inner shaft and the outer sheath, located between distal and proximal stent makers on the inner shaft. The stent expands to its unconstrained diameter when released from the deployment catheter into the carotid artery. Upon deployment the stent forms an open lattice and pushes outward on the luminal surface, helping to maintain the patency of the artery. Due to the self-expanding behavior of nitinol, the stents are indicated for placement into vessels that are 1-2mm smaller in diameter than the unconstrained diameter of the stent.

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code NIM·November 14, 2019

    Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code LZH·December 26, 2019

    BD UF PEN 32GX4MM 100 NANO Item Number: 4292272

    FDA Recall
    Open, Classified ·Cardinal Health Inc.·Product code FMI·March 16, 2021