BEUDAMED
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    HI-TORQUE SUPRA CORE 35 GUIDE WIRE WITH MICROGLIDE COATING

    FDA Adverse Event
    Malfunction ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code DQX·March 28, 2006

    CORAIL2 ANTERIOR BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code HTQ·October 23, 2020

    X-SERIES HUDSON HTQ RMER ATTACH

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL SA·Product code GEY·January 2, 2025

    X-SERIES ZIMMER/HUDSON HTQ RMER ATTACH

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL SA·Product code GEY·January 2, 2025

    Zimmer TM-400 Broach Handle; Part No. 96-210-10001. The product is a surgical instrument for use in conjunction with Zimmer TM-400 Trabecular Metal implants during spinal surgery. The Broach Handle threads onto various broaches and trial implants. The handle with these broaches or trials attached is used to prepare and measure a vertebral space to accept a TM-400 Trabecular Metal implant.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code HTQ·April 29, 2009

    Rejuvenate Broach Catalog No: 1601-1005, 1601-1006, 1601-1007, 1601-1008, 1601-1009, 1601-1010 Stryker Orthopaedics, Mahwah, NJ. 07430 Contours the proximal femur to the geometry of the stem to provide a complimentary fit of the stem to the bone.The broaches are designed with a series of teeth that are intended to seat against highly densified cancellous bone for the interference press-fit in the uncemented application.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HTQ·January 25, 2008

    Zimmer Nexgen Complete Knee Solution Fluted Stemmed Tibial Broach, Size 7, 8, nonsterile; REF 5997-61-07. A reusable cutting instrument that is used in total knee arthroplasty surgery.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code HTQ·March 13, 2009

    Linear Straight Broach Handle (Rasp Handle) (Greatbatch Part # 510397; DJO Surgical Inc., # 803-03-159) and EZ Clean" Linear Broach Handle Greatbatch Part # T11824, DJO Surgical Inc. # 803-03-059).

    FDA Recall
    Terminated ·Greatbatch Medical·Product code HTQ·April 23, 2017

    Foundation Knee System Instrumentation, Tibial Broach Assembly. Used in conjunction with the Tibial Sizing Template and Tibial Broach Guide to prepare the resected tibial plateau for acceptance of a keeled tibial baseplate stem.

    FDA Recall
    Terminated ·Product code HTQ·April 21, 2011

    EXTRA CURVED BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HTQ·November 3, 2016

    SUMMIT BROACH EXTRACTOR

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HTQ·November 9, 2016

    EXTRA CURVED BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTQ·December 19, 2016

    CORAIL2 STRAIGHT BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HTQ·October 24, 2016

    SUMMIT UNIVERSAL BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTQ·November 22, 2016

    UNKNOWN DEPUY BROACH

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HTQ·November 17, 2016

    CORAIL2 ANTERIOR BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HTQ·November 8, 2016

    BROACH CORAIL AMT 10

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTQ·October 31, 2016

    CORAIL BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HTQ·December 21, 2016

    HUMORAL BROACH SZ 1

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code HTQ·March 21, 2012

    SHOULDER INSTRUMENT

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HTQ·February 13, 2009