Recall
FDAHealthJanuary 2, 2026

Alphatec Spine, Inc. — ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
January 2, 2026

U.S. Nationwide distribution in the states of AZ, CA, FL, IL, IN, MA, MI, MO, NC, NH, NY, TN, TX, and VA.

What's affected?

Product
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; 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 instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Lot code
EM56693

Additional details

Model/Catalog Number: 267-01-000-10-N UDI-DI code: 00190376541471 Lot Number: EM56693

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 15 units.

View original FDA notice →

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