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    ZIMMER MANUFACTURING B.V.

    FDA registration
    ZIMMER MANUFACTURING B.V.·23 products·🇺🇸 United States

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, BUILDING #2·Product code JWH·December 23, 2015

    Bone Screw, self-tapping The Trilogy shells are available in three configurations; uni, multi, and cluster-holed. The multi and cluster-holed shells allow for the use of screws to provide additional fixation and security, particularly in those case where acetabular bone stock is deficient. The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing primary or revision surgery for rehabilitating hips damaged as a result of noninflammatory degenerative joint disease (NIDJD) or its composite diagnoses of osteoarthritis, avascular necrosis, protrusio acetabuli, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant.

    FDA Recall
    Terminated ·Zimmer Manufacturing B.V.·Product code LPH·November 21, 2014

    TRABECULAR METAL SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JDI·January 6, 2016

    NEXGEN CR-FLEX GSF FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, BUILDING #2·Product code JWH·February 29, 2016

    CONTINUUM TM SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LZO·November 25, 2015

    ZIMMER ALUMINA CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code MRA·March 23, 2016

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, BUILDING #2·Product code JWH·February 10, 2016

    Zimmer TIV Self Tap Screw, 40 mm. Manufactured by Zimmer Manufacturing B.V., A Subsidiary of Zimmer, Inc., Warsaw, IN; Item No. 48231904000. NOTE: This product is not sold in the United States. The device is used to attach healing plates to long bones for stabilization of fractures during the normal healing process. Devices are individually packaged and sold sterile.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code HWC·December 12, 2008

    Zimmer TIV Self Tap Screw, 42 mm. Manufactured by Zimmer Manufacturing B.V., A Subsidiary of Zimmer, Inc., Warsaw, IN; Item No. 48231904200. NOTE: This product is not sold in the United States. The device is used to attach healing plates to long bones for stabilization of fractures during the normal healing process. Devices are individually packaged and sold sterile.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code HWC·December 12, 2008

    KINECTIV MODULAR NECK

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code MEH·January 25, 2016

    UNKNOWN NEXGEN CR-FLEX FEMORALCOMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC.·Product code JWH·January 15, 2014

    TRILOGY ACETABULAR LINER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWB·August 26, 2010

    PRESSFIT FEM ST FX 16 X 1

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014

    ZIMTRON 6 DEG 22 HEADS

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014

    HGP II ACETABULAR CUP MOD

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014

    ASIA ONE-PIECE LAG SCREW

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014

    CONTINUUM TM SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LZO·August 24, 2015

    KINECTIV MODULAR NECK

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code KWA·March 28, 2016

    FEM HD ION (various sizes)

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014