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    Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code JWH·August 15, 2014

    Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code JWH·August 15, 2014

    Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments. Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA A subsidiary of Stryker Corporation. Made in USA. Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZIEU Cedex France The Baseplate Impactor Extractor is intended to securely attach to the tibial baseplate or baseplate trial for impaction and extraction during surgery.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code JWH·February 23, 2013

    Stryker Radius Locking Caps, Catalog Number: 486610000, Manufactured by Stryker Spine SAS Z.I. Marticot - 33610 Cestas France.,Distributed by Howmedica Osteonics Corp. 325 Corporate Drive, Mahway, NJ 07430

    FDA Recall
    Terminated ·Stryker Spine·Product code NKB·July 10, 2007

    Scorpio Fixed Femoral A/P Sizing Guide; non-sterile instruments; Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430; A subsidiary of Stryker Corporation The A/P sizer is designed to set the desired external rotation and to provide adjustment of the anterior/posterior position when needed.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·September 27, 2010

    Scorpio Adjustable Femoral A/P Sizing Guide Assembly; non-sterile instruments; Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430; A subsidiary of Stryker Corporation The A/P sizer is designed to set the desired external rotation and to provide adjustment of the anterior/posterior position when needed.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·September 27, 2010

    AlloCraft DBM with Syringe Assembly, 10 CC, LifeCell Corporation, Branchburg, NJ 08876 , Distributed by Stryker Spine

    FDA Recall
    Terminated ·LifeCell Corporation·Product code MQV·October 17, 2007

    Stryker Howmedica Osteonics; Stryker T2 Humerus System Teflon Tube, sterile; REF 1806-0073S The T2 Nailing System is designed to treat complex fractures in Humeral, Femoral, Tibial and Ankle applications. The Teflon Tube is an optional instrument used to exchange the Ball Tip Guide Wire with the Smooth Tip Guide Wire once reaming is completed. Stryker Stryker Trauma GmbH 24232 Schonkirchen, Germany distributed in USA by: Howmedica Osteonics Corp., 235 Corporate Drive,

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·August 6, 2012

    Stryker T2 Locking Screw, Fully threaded; 05 x 70mm, Catalog Number: 1896-5070S, Sterile, Qty: 1,Stryker Trauma GMbH, 24232 Schonkirchen, Germany Distributed in the United States by Howmedica Osteonics Corp.; 325 Corporate Drive, Mahwah, NJ 07430

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·September 27, 2007

    AlloCraft DBM with Syringe Assembly, 5CC, Catalog/Reorder Number: 653005, LifeCell Corporation, Branchburg, NJ 08876 , Distributed by Stryker Spine

    FDA Recall
    Terminated ·LifeCell Corporation·Product code MQV·October 17, 2007

    Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. Hip prosthesis component. The RESTORATION Acetabular Wedge Augments provide multiple options to address the wide range of bone deficiencies encountered in acetabular revision. The augments provide support for the shell in the acetabulum with superior and/or posterior defects.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LPH·August 15, 2014

    Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 20 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 25 mm; Sterile; Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 60 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 30 mm; Sterile; Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 35 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 16 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 45 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009

    Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 35 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HWC·June 26, 2009