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Recall Observatory FDA recall evidence

Device product

Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T, ST241T, ST242T, ST243T, ST244T, and ST245T). The S4 Spinal System is intended for anterior/anterolateral and posterior, non-cervical pedicle and non-pedicle fixation. Fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion using autograft or allograft. The device is indicated for treatment of the following acute and chronic instabilities or deformities: 1 - degenerative disc disease, 2 - spondylolisthesis, 3 - trauma, 4 - spinal stenosis, 5 - deformities or curvatures, 6 - tumor, 7 - pseudoarthrosis, and 8 - failed previous fusion.

Z-2333-2012

July 25, 2012

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 62842
Status
Terminated
Classification
Class II
Quantity
5
Official record key
device-enforcement:Z-2333-2012

Official wording

Reason: There is a possibility that the screw channel that holds the rod in place may be out of tolerance. When the depth of the channel is not deep enough, the rod may not be able to provide ample compression on the insert preventing the screw head from locking down to the bone screw.

Code information: All distributed lots and serial numbers

Distribution pattern: Nationwide Distribution-including the states of IL, MN, NV, OK, and TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is a possibility that the screw channel that holds the rod in place may be out of tolerance. When the depth of the channel is not deep enough, the rod may not be able to provide ample compression on the insert preventing the screw head from locking down to the bone screw.