BEUDAMED
    4,346 results · 35ms · Sources: EU EUDAMED, US FDA

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    REMANUFACTURED BED

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·April 30, 2009

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 13, 2009

    SPINBRUSH¿ PRO WHITENING¿ POWERED TOOTHBRUSH

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·February 5, 2013

    O-ARM O2 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·SANMINA -SCI SYSTEMS·Product code OWB·March 27, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 23, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 31, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 24, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 23, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 23, 2024

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 23, 2024

    INTRALASE FS LASER

    FDA Adverse Event
    Malfunction ·INTRALASE CORP.·Product code GEX·October 18, 2002

    REMSTAR PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·June 25, 2024

    REMSTAR PRO

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·June 25, 2024

    Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient under the direction or supervision physician or other certified healthcare professional.

    FDA Recall
    Open, Classified ·Zyno Medical LLC·Product code FRN·September 30, 2024

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 12, 2017

    DUROM ACETABULAR COMPONENT 50/44 CODE J

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·February 12, 2014

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·April 30, 2020

    UNKNOWN IMPLANTABLE NEUROSTIMULATO

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 10, 2015

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·June 26, 2024

    ORTHOSIS, CERVICAL PEDICLE SCREW SPINAL FIXATION

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·April 23, 2019