BEUDAMED
    28 results · 21ms · Sources: EU EUDAMED, US FDA

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    CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·May 12, 2021

    CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·October 24, 2023

    CardioQuip, Modular Cooler-Heater 1000(i), Standard Unit, Model: MCH-10RMS, CE 2797, UDI: (01) 00860000846127

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·May 12, 2021

    CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·October 19, 2023

    CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·May 12, 2021

    3T Heater Cooler System, REF: 16-02-85

    FDA Recall
    Open, Classified ·LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany·Product code DWC·August 3, 2023

    CardioQuip, Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid, Model: MCH-11TEC,CE 2797, UDI: (01) 00860000846134

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·May 12, 2021

    CardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·October 19, 2023

    CardioQuip Modular Cooler-Heater, Model: MCH-1000(i), Power: 115V-60Hz, 16A

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·October 24, 2023

    CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.

    FDA Recall
    Open, Classified ·CardioQuip, LLC·Product code DWC·June 24, 2021

    DAC 044 115cm, Catalog: 90760

    FDA Recall
    Open, Classified ·Stryker Neurovascular·Product code DQY·April 23, 2024

    PDSIIVIO30IN(75CM)USP6-0(M0.7)D/AC-1

    FDA Recall
    Open, Classified ·Ethicon Endo Surgery, LLC·Product code NEW·March 7, 2025

    PDSPLUSVIO30IN(75CM)USP6-0(M0.7)D/AC-1MP

    FDA Recall
    Open, Classified ·Ethicon Endo Surgery, LLC·Product code NEW·March 7, 2025

    The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker on the distal end and a luer hub on the proximal end. The catheter shaft has a hydrophilic coating to reduce friction during use. Device dimensions and configuration are shown on the product label. A rotating hemostasis valve with side-arm adapter is provided with each catheter. The rotating hemostasis valve is typically y shaped with a female luer lock and a manual hemostasis valve. The female port allows for aspiration and contrast injections while the hemostasis valve allows direct arterial access when using other devices such as guidewires and/or interventional devices.

    FDA Recall
    Open, Classified ·Stryker Neurovascular·Product code DQY·April 3, 2024

    Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART.

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OEZ·February 21, 2025

    Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number C-TCCSB-500-UNI, Order Number G32193; Reference Part Number C-TCCSB-500-UNI-01, Order Number G47665.

    FDA Recall
    Open, Classified ·Cook Incorporated·Product code BWC·March 5, 2026

    CombiDiagnost R90; Model Number: 709031;

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025

    DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code KPR·October 1, 2025

    Radiography 7300 C; Model Number: 712037;

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code KPR·October 1, 2025

    ProxiDiagnost N90; Model Number: 706110;

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025