BEUDAMED
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    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·April 10, 1997

    MARK II INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·September 13, 1996

    ENDOPATH ETS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·July 22, 2009

    HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code LFL·July 22, 2009

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·October 28, 1996

    HOLDER, NEEDLE, 7 INCH,CODMAN, RYDER, CLASSIC PLUS,

    FDA Adverse Event
    Malfunction ·CODMAN·Product code FCG·April 4, 2012

    IPP INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·April 9, 1997

    MARK II INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·March 19, 1997

    GFS INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·November 8, 1996

    ALPH I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·August 7, 1997

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·March 25, 1997

    ELEKTA SYNERGY

    FDA Adverse Event
    Malfunction ·ELEKTA LIMITED·Product code IYE·February 21, 2024

    AUTO SUTURE ENDO CLIP 5MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORPORATION·Product code GCJ·December 22, 1997

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·September 19, 1997

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·November 12, 1996

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·March 25, 1997

    ALPHA I

    FDA Adverse Event
    Injury ·MENTOR CORPORATION - MINNESOTA DIVISION·Product code FHW·June 22, 2006

    USSC BIOSYN 3/0

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAN·June 27, 1997

    ALPHA I

    FDA Adverse Event
    Injury ·MENTOR CORORATION-MINNESOTA DIVISION·Product code FHW·September 8, 2006

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·July 9, 1997