Alphatec Spine, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1343-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 2, 2026

Date Posted: February 18, 2026

Recall Number: Z-1343-2026

Event ID: 98251

Reason for Recall:

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

Status: Ongoing

Product Quantity: 15 units

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated