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Recall Observatory FDA recall evidence

Device product

Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS Spinal Fixation System is intended for posterior, noncervical pedicle fixation, T1-S2. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion. The device is indicated for all the following indications: degenerative disc disease (ODD) (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e. fracture or dislocation); spinal stenosis; deformities or curvatures (i.e. scoliosis, kyphosis, and /or lordosis); tumor; pseudoarthrosis; and failed previous fusion. The Streamline MIS instrumentation, when used with the Streamline MIS Spinal Fixation System, is indicated to provide the surgeon with a minimally invasive approach for posterior spinal surgery.

Z-2616-2014

June 14, 2013

Class II

Product summary

Firm
PIONEER SURGICAL TECHNOLOGY, INC.
Event
Event 69036
Status
Terminated
Classification
Class II
Quantity
9
Official record key
device-enforcement:Z-2616-2014

Official wording

Reason: The affected fixed rod holders did not allow the instrument to lock down on the spinal rod.

Code information: Lot number: 148062, 148440

Distribution pattern: Nationwide Distribution including TX, CA, IL, and FL.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The affected fixed rod holders did not allow the instrument to lock down on the spinal rod.