Z-2616-2014 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- September 17, 2014
- Initiation Date
- June 14, 2013
- Termination Date
- September 30, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9
Product Description
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.
Reason for Recall
The affected fixed rod holders did not allow the instrument to lock down on the spinal rod.
Distribution Pattern
Nationwide Distribution including TX, CA, IL, and FL.
Code Information
Lot number: 148062, 148440