BEUDAMED
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    Filters Status: Malfunction ×

    J+J

    FDA Adverse Event
    Malfunction ·J + J·Product code KWB·October 22, 2002

    CURVED ACETABULAR CUP INSERTER

    FDA Adverse Event
    Malfunction ·DEPUY J+J·Product code LXH·October 28, 2009

    PROTECTIV PLUS CATHETER

    FDA Adverse Event
    Malfunction ·J+J MEDICAL·Product code FOZ·February 19, 2001

    J & J CODMAN

    FDA Adverse Event
    Malfunction ·JARIT·Product code KWQ·June 23, 2003

    J & J STENT

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON INTERVENTIONAL SYSTEMS CO.·Product code MAF·January 30, 1996

    LIGAMAX

    FDA Adverse Event
    Malfunction ·J & J ETHICON·Product code FZP·January 26, 2010

    ATS 45

    FDA Adverse Event
    Malfunction ·ETHICON, J & J·Product code GDW·June 2, 2014

    8 FR VISTA BRITE TIP GUIDE CATH

    FDA Adverse Event
    Malfunction ·CORDIS/J & J·Product code DYB·February 3, 2004

    ETHICON

    FDA Adverse Event
    Malfunction ·ETHICON (J AND J)·Product code FZP·August 14, 2003

    ETHICON

    FDA Adverse Event
    Malfunction ·ETHICON (J AND J)·Product code FZP·August 14, 2003

    (JELCO)PROTECTIV PLUS

    FDA Adverse Event
    Malfunction ·J+J MEDICAL INC·Product code FOZ·November 9, 2000

    JELCO

    FDA Adverse Event
    Malfunction ·J & J MEDICAL·Product code FOZ·June 20, 1997

    STAPLER - ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON J & J·Product code KOG·September 24, 2002

    ETHICON

    FDA Adverse Event
    Malfunction ·ETHICON J & J·Product code GCJ·June 10, 2011

    ETHICON

    FDA Adverse Event
    Malfunction ·J & J ETHICON·Product code GCJ·June 10, 2011

    DENVER PERITONEO - VENOUS SHUNT

    FDA Adverse Event
    Malfunction ·J & J CODMAN·Product code FIQ·July 1, 1992

    J&J CODMAN

    FDA Adverse Event
    Malfunction ·J & J CODMAN·Product code JXG·June 20, 2002

    ENDOPOUCH RETRIEVER

    FDA Adverse Event
    Malfunction ·ETHICON ENDOSURGERY / J+J·Product code MDM·August 4, 2010

    UNKNOWN J & J PATELLA

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·June 10, 2005

    UNK J & J PATELLA

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·February 7, 2003