FDADecember 15, 2024device

Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, nonsterile; (2) Calibrate CCX-O, 7 x 10 x 25mm 10 degrees, Part #325-07102510, nonsterile; (3) Calibrate CCX-O, 7 x 10 x 25mm 15 degrees, Part #325-07102515, no...

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

The hazard

Complaints have been received regarding post-operative implant collapse.

What to do

FDA enforcement status: Ongoing

Brands named

alphatec spinealphatec

UPCs

001903765333080019037653296700190376532974001903765329980019037653300100190376533018001903765330490019037653305600190376533322001903765333390019037653336000190376533377

Recall history

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

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