FDAJanuary 2, 2026device

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use i...

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

The hazard

Due a design issue where the navigated array connection geometry is incorrect.

What to do

FDA enforcement status: Ongoing

Brands named

alphatec spinealphatec

UPCs

00190376476179

Recall history

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

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