BEUDAMED
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    DWO CORNING BREAST IMPLANT

    FDA Adverse Event
    Injury ·DOW CORNING·Product code FTR·November 14, 2001

    The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These products were produced for DeWALT and Stanley by a contract manufacturer.

    FDA Enforcement
    Class II ·Ongoing·STANLEY BLACK & DECKER INC.·January 8, 2020

    CHIBA BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK INC.·Product code DWO·May 19, 2014

    KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DWO·May 10, 2010

    OSTYCUT BONE BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015

    KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DWO·May 3, 2012

    ACKERMANN BONE BIOPSY NEEDLE SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DWO·April 19, 2012

    KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DWO·April 30, 2012

    COOK

    FDA Adverse Event
    Injury ·COOK INC.·Product code DWO·February 19, 2002

    OSTEO-SITE BONE BIOPSY NEEDLE SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DWO·February 19, 2002

    OSETO-SITE BONE BIOSPY NEEDLE

    FDA Adverse Event
    Injury ·COOK INC·Product code DWO·March 6, 2002

    PERCUTANEOUS ENTRY NEEDLE

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DWO·February 22, 2002

    RING DRAINAGE CATHETER NEEDLE SET

    FDA Adverse Event
    Malfunction ·COOK MEDICAL·Product code DWO·February 13, 2012

    BONE MARROW NEEDLE (J TYPE)

    FDA Adverse Event
    Injury ·MANAN MEDICAL PRODUCTS, INC., DBA ANGIOTECH·Product code DWO·March 14, 2012

    OSTYCUT DISPOSABLE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·January 17, 2012

    OSTYCUT BONE BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015

    ROSENTHAL NEEDLE 16G X 2"

    FDA Adverse Event
    Malfunction ·POPPER PRECISION INSTRUMENTS·Product code DWO·June 16, 2000

    1213649-2000-00001

    FDA Adverse Event
    Other ·Product code DWO·June 16, 2000

    KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DWO·October 13, 2009

    OSTYCUT DISPOSABLE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·November 23, 2009