BEUDAMED
    3,921 results · 22ms · Sources: EU EUDAMED, US FDA

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    STELLA CONTACTS

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LPL·August 11, 2023

    Shiley FlexTra brand Flexible Dual-Cannula Tracheostomy Tube, Models: 358060, Size 6, FlexTra Cuffed; 358070, Size 7, FlexTra Cuffed; 358080, Size 8, FlexTra Cuffed; 358090, Size 9, FlexTra Cuffed; 358100, Size 10, FlexTra Cuffed; 359060, Size 6, FlexTra Uncuffed; 359070, Size 7, FlexTra Uncuffed; 359080, Size 8, FlexTra Uncuffed; 359090, Size 9, FlexTra Uncuffed; 359100, Size 10, FlexTra Uncuffed, Tyco Healthcare/Nellcor is currently responsible for Research and Development for this product. Tyco Healthcare/MMJ S.A. De C.V., Cuidad Juarez, Mexico manufactures the FlexTra Tracheostomy Tube. The product is sterilized at Sterigenics, located at Santa Teresa, New Mexico.

    FDA Recall
    Terminated ·Nellcor Puritan Bennett·Product code JDH·December 9, 2004

    CONTOUR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·October 28, 2016

    REDAPT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·October 24, 2016

    TNDM BP SHL/XLPE LNR 41OD 26ID

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·October 25, 2016

    TANDEM BIPOLAR SHELL/XLPE LINER 42MM OD 26MM ID

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·October 25, 2016

    HIP PROSTHESIS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code JDH·August 14, 2015

    HIP PROSTHESIS SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·September 8, 2015

    HIP PROSTHESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·August 12, 2015

    HIP PROSTHESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·July 17, 2015

    REF FSO 5 50MM OD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·July 15, 2015

    SYNERGY

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC·Product code JDH·February 27, 2012

    1020279-2012-00073

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC·Product code JDH·February 7, 2012

    FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·January 26, 2012

    UNKNOWN

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·January 4, 2012

    1020279-2012-00182

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC·Product code JDH·March 21, 2012

    BIPOLAR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·February 6, 2012

    FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BROOKS MANUFACTURING SITE·Product code JDH·March 27, 2012

    REFLECTION

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·January 23, 2012

    TANDEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·February 2, 2012