BEUDAMED
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    SCRDRIVER ANGL

    FDA Adverse Event
    Injury ·SYNTHES HAGENDORF·Product code LRZ·October 12, 2017

    STRAIGHT SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code LRZ·August 28, 2020

    CAPTIVE HEX SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ENDIUS, INC.·Product code LRZ·September 20, 2004

    ZIMMER

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code LRZ·April 5, 1993

    SKYLINE CAM LOCKING

    FDA Adverse Event
    Malfunction ·DEPUY SPINE·Product code LRZ·September 28, 2011

    ERISMA-LP MIS

    FDA Adverse Event
    Malfunction ·CLARIANCE SAS·Product code LRZ·September 13, 2023

    STRAIGHT SCREWDRIVER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LRZ·February 20, 2017

    MANUAL SCREWDRIVER (MEDIUM) STST 0.9

    FDA Adverse Event
    Injury ·JJGC S.A.·Product code LRZ·February 16, 2023

    SKYLINE CAM LOCKING

    FDA Adverse Event
    Malfunction ·DEPUY SPINE·Product code LRZ·October 19, 2011

    CANNULATED SCREW DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code LRZ·December 30, 1992

    SCREW DVO DRIVE

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code LRZ·December 2, 1992

    ZIMMER

    FDA Adverse Event
    Injury ·ZIMMER·Product code LRZ·July 16, 1993

    TORQUE-SHANK, T7X80 CANNULATED, AO CONNECTOR

    FDA Adverse Event
    Malfunction ·I.T.S. GMBH·Product code LRZ·January 9, 2019

    SCREWDRIVER HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES - A-O·Product code LRZ·July 31, 1992

    Tray Set containing multiple instruments and may contain the flexible bone awl, flexible drill and/or flexible screw driver in varying amounts depending on order. Tray set is not sealed. These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems. Tray catalog number is: Tray designated as ST0485-037.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015

    Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015

    Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N 129735ND). Indicated for use in fixation of fractures, osteotomies and arthrodesis of the first metatarso-phalangeal joint.

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code LRZ·February 1, 2013

    Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015

    Genesys spine, Binary Screwdriver, GCP221, component of the Binary Anterior Cervical Plating System The Genesys Spine Binary Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine. It is to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to C7). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), spondylolisthesis, trauma (i.e. fractures or dislocations), tumors, deformity (defined as kyphosis, lordosis, or scoliosis),pseudoarthrosis, failed previous fusion, and/or spinal stenosis.

    FDA Recall
    Terminated ·Genesys Orthopedics Systems, LLC 1250 S Capital of Texas Hwy Ste 600 Bldg # 3 West Lake Hills TX 78746-6446·Product code LRZ·November 5, 2015

    Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015