BEUDAMED
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    stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 6 RM/LL), REF 170616, intended for use in a Partial Knee Arthroplasty surgical procedure

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code HSX·March 10, 2023

    stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial Knee Arthroplasty surgical procedure

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code HSX·March 10, 2023

    AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

    FDA Recall
    Open, Classified ·ZOLL Circulation, Inc.·Product code DRM·September 22, 2022

    LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

    FDA Recall
    Open, Classified ·Jolife AB Scheelevagen 17 Ideon Science Park Lund Sweden·Product code DRM·May 21, 2025

    RMU-2000 Automated Chest Compression Device

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code DRM·July 12, 2024

    Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

    FDA Recall
    Open, Classified ·Remel Europe Ltd. Clipper Boulevard West Ken Dartford United Kingdom·Product code GRM·March 25, 2026

    Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number: 8700-001070-1) Software Version: Version 2.0.1 Product Description: The AutoPulse Resuscitation System Model 200 is an automated, portable, battery powered device that compresses the chest of an adult human as an adjunct to manual CPR. Component: N/A

    FDA Recall
    Open, Classified ·ZOLL Circulation, Inc.·Product code DRM·March 4, 2025

    LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

    FDA Recall
    Open, Classified ·Jolife AB Scheelevagen 17 Ideon Science Park Lund Sweden·Product code DRM·April 13, 2026