BEUDAMED
    6,795 results · 49ms · Sources: EU EUDAMED, US FDA

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    UNK GEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 1, 2023

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 31, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 31, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 31, 2019

    UNKNOWN HIP ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 31, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 31, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 31, 2019

    SEMI-RIDID SCISSORS

    FDA Adverse Event
    Malfunction ·CIRCON ACMI·Product code JOK·January 22, 2002

    SEMI-RIGID SCISSORS

    FDA Adverse Event
    Malfunction ·CIRCON ACMI·Product code JOK·January 4, 2002

    ETHICON

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON COMPANY·Product code JOK·February 22, 1994

    MARLOW NU TIP

    FDA Adverse Event
    MARLOW CO.·Product code JOK·January 31, 1995

    SCANLAN INTERNATIONAL, INC.

    FDA Adverse Event
    Injury ·SCANLAN INTL., INC.·Product code JOK·April 21, 2004

    INTUITIVE

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL·Product code JOK·September 30, 2009

    72-7000 CORD CLAMP CUTTER

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code JOK·April 22, 2002

    72-7000 CORD CLAMP CUTTER

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code JOK·April 22, 2002

    CENTURION

    FDA Adverse Event
    Malfunction ·CENTURION MEDICAL PRODUCTS, LP·Product code JOK·March 19, 2026

    GENICON

    FDA Adverse Event
    GENICON·Product code JOK·June 28, 2017

    UNKNOWN SOLITAIRE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·October 24, 2023

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 31, 2019

    MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code JOK·April 30, 2024