WhichRecall
Class IIReported 2026-02-18

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.

Recalled by Alphatec Spine, Inc.

Reason for Recall

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

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Recall Number
Z-1343-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-01-02
Reported
2026-02-18
Distribution
U.S. Nationwide distribution in the states of AZ, CA, FL, IL, IN, MA, MI, MO, NC, NH, NY, TN, TX, and VA.
Code Info
Model/Catalog Number: 267-01-000-10-N UDI-DI code: 00190376541471 Lot Number: EM56693
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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