BEUDAMED
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    Stryker XIA 3 Polyaxial Screw, 8.5mm x 65 mm. Catalog Number: 482318565. Not Sterile; Manufactured by Stryker Spine, SA, Cestas, France. Distributed in the USA by Stryker Spine, Allendale, NJ Intended for use in the noncervical spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code NKB·December 30, 2009

    Stryker Mantis Rod Inserter Assembly Manufactured by: Stryker Spine SAS Z. I. Marticot - 33610 - Cestas France; Distributed in the USA by: Stryker Spine 2 Pearl Court. Allendale, NJ 07401-1677 USA Stryker Mantis Rod Inserter Inner Shaft Manufactured by: Stryker Spine SAS Z. I. Marticot - 33610 - Cestas France; Distributed in the USA by: Stryker Spine 2 Pearl Court. Allendale, NJ 07401-1677 USA IS2097MAN Mantis Rod Inserter Shaft Used to facilitate insertion and delivery of a Mantis rod.

    FDA Recall
    Terminated ·Stryker Spine·Product code HSB·June 24, 2011

    Stryker 9 MM AVS TL Trial Spacer; Catalog number: 48389409. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 11 MM AVS TL Trial Spacer; Catalog number: 48389411. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 17 MM AVS TL Trial Spacer; Catalog number: 48389417 Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 14 MM AVS TL Trial Spacer; Catalog number: 48389414. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 7 MM AVS TL Trial Spacer; Catalog number: 48389407. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 13 MM AVS TL Trial Spacer; Catalog number: 48389413. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 10 MM AVS TL Trial Spacer; Catalog number: 48389410. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 12 MM AVS TL Trial Spacer; Catalog number: 48389412. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 18 MM AVS TL Trial Spacer; Catalog number: 48389418. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 16 MM AVS TL Trial Spacer; Catalog number: 48389416. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 8 MM AVS TL Trial Spacer; Catalog number: 48389408. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Stryker 15 MM AVS TL Trial Spacer; Catalog number: 48389415. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine.

    FDA Recall
    Terminated ·Stryker Spine·Product code MDM·May 13, 2010

    Reflex Hybrid 4.0 x 14 mm Variable, Self-Tapping Bone Screw (Non- sterile). Manufactured by Stryker Spine SAS, Cestas, France. Distributed in USA by Howmedica Osteonics, Mahwah, NJ. The bone screw (Reference # 48694014) is a 04.0 x 14mm used to attach the Reflex Hybrid Anterior Cervical Plate (ACP) to the anterior surface of the spine. The intended use of the system is as an aid in cervical spinal fusion through unilateral fixation.

    FDA Recall
    Terminated ·Stryker Spine·Product code KWQ·August 18, 2008

    Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine Manufactured by : Stryker Spine SAS France Used to facilitate insertion of the Aero-AL cage into the disc space.

    FDA Recall
    Terminated ·Stryker Spine·Product code LXH·December 18, 2015

    Stryker Xia Precision System; Jam Shidi 10 Gauge 5 inch; Sterile; Manufactured for: Stryker Spine SAS, Cestas, France; Distributed in the US by Howmedica Osteonics Corp, 325 Corporate Drive, Mahwah, NJ. Intended for use as a manual surgical instrument during percutaneous posterior, non-cervical pedicle fixation.

    FDA Recall
    Terminated ·Stryker Spine·Product code LXH·January 18, 2010

    Stryker Xia Precision System; Jam Shidi 10 Gauge 9 inch; Sterile; Manufactured for: Stryker Spine SAS, Cestas, France; Distributed in the US by Howmedica Osteonics Corp, 325 Corporate Drive, Mahwah, NJ. Intended for use as a manual surgical instrument during percutaneous posterior, non-cervical pedicle fixation.

    FDA Recall
    Terminated ·Stryker Spine·Product code LXH·January 18, 2010

    Stryker Xia Precision System; Jam Shidi 13 Gauge 5 inch; Sterile; Manufactured for: Stryker Spine SAS, Cestas, France; Distributed in the US by Howmedica Osteonics Corp, 325 Corporate Drive, Mahwah, NJ. Intended for use as a manual surgical instrument during percutaneous posterior, non-cervical pedicle fixation.

    FDA Recall
    Terminated ·Stryker Spine·Product code LHX·January 18, 2010

    Stryker Xia Precision System; Jam Shidi 11 Gauge 5 inch; Sterile; Manufactured for: Stryker Spine SAS, Cestas, France; Distributed in the US by Howmedica Osteonics Corp, 325 Corporate Drive, Mahwah, NJ. Intended for use as a manual surgical instrument during percutaneous posterior, non-cervical pedicle fixation.

    FDA Recall
    Terminated ·Stryker Spine·Product code LXH·January 18, 2010