FDA Enforcement
Class II
Ongoing
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 instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Recall: Z-1342-2026
·
Reported February 18, 2026
Enforcement
- Recall Number
- Z-1342-2026
- Event ID
- 98251
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Alphatec Spine, Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- February 18, 2026
- Initiation Date
- January 2, 2026
- Classification Date
- February 11, 2026
- Address
- 1950 Camino Vida Roble, N/A, Carlsbad, CA, 92008-6505, United States
Description
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 instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Reason
Due a design issue where the navigated array connection geometry is incorrect.
Code Info
Model/Catalog Number: 266-01-000-10-N UDI-DI code: 00190376476179 Lot Number: EM49968
Distribution
U.S. Nationwide distribution in the states of AZ, CA, FL, IL, IN, MA, MI, MO, NC, NH, NY, TN, TX, and VA.
Quantity
7 units