FDAMarch 11, 2015device

Xpress System Pedicle Screw Assembly, 5.5 x 55mm. An internal fixation device for spinal surgery consisting of rods, pedicle screw assemblies (screw, cap, yoke) and cross bar connector assemblies.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

One lot of instruments have etched on the Yoke of the Pedicle Screw a laser marking size of 7.5 x 55mm instead of 5.5 x 55mm as described on the product label.

What to do

FDA enforcement status: Terminated

Brands named

x spine systems

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Xpress System Pedicle Screw Assembly, 5.5 x 55mm. An internal fixation device for spinal surgery consisting of rods, pedicle screw assemblies (screw, cap, yoke) and cross bar connector assemblies. — Recall Details · AllClear