Alphatec Spine recalls

Alphatec Spine appears in 46 official U.S. recall notices indexed by RecallRadar, most recently on 2026-07-29.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System
  FDA Device · Class II · 2026-07-29 · Alphatec Spine
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471
  FDA Device · Class II · 2026-02-18 · Alphatec Spine
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179
  FDA Device · Class II · 2026-02-18 · Alphatec Spine
• Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, no…
  FDA Device · Class II · 2025-02-05 · Alphatec Spine
• IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x 25 mm 132-10-85-300…
  FDA Device · Class II · 2024-03-06 · Alphatec Spine
• LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System
  FDA Device · Class II · 2023-09-06 · Alphatec Spine
• Disc Preparation instruments contained in the following products: CI-11050-08102515 Longer IdentiTi PO Trial Tip, 11A X 8P X 10 X 25mm, 15¿…
  FDA Device · Class II · 2022-11-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0236 Insignia, ACP, 2-Level, 36 mm, Rx Only, Non-Sterile, UDI: (01)00190376268385
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0119, Insignia, ACP, 1-Level, 19 mm, Rx Only, Non-Sterile, UDI: (01)00190376268453
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0244 Insignia, ACP, 2-Level, 44 mm, Rx Only, Non-Sterile, UDI: (01)00190376268507
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0250 Insignia, ACP, 2-Level, 50 mm, Rx Only, Non-Sterile, UDI: (01)00190376268538
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0352 Insignia, ACP, 3-Level, 52 mm, Rx Only, Non-Sterile, UDI: (01)00190376268576
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0242 Insignia, ACP, 2-Level, 42 mm, Rx Only, Non-Sterile, UDI: (01)00190376268415
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0474 Insignia, ACP, 4-Level, 74 mm, Rx Only, Non-Sterile, UDI: (01)00190376268699
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0362 Insignia, ACP, 3-Level, 62 mm, Rx Only, Non-Sterile, UDI: (01)00190376268620
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0240 Insignia, ACP, 2-Level, 40 mm, Rx Only, Non-Sterile, UDI: (01)00190376268408
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0118, Insignia, ACP, 1-Level, 18 mm, Rx Only, Non-Sterile, UDI: (01)00190376268446
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0356 Insignia, ACP, 3-Level, 56 mm, Rx Only, Non-Sterile, UDI: (01)00190376268590
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0117, Insignia, ACP, 1-Level, 17 mm, Rx Only, Non-Sterile, UDI: (01)00190376268439
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0468 Insignia, ACP, 4-Level, 68 mm, Rx Only, Non-Sterile, UDI: (01)00190376268675
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0124, Insignia, ACP, 1-Level, 24 mm, Rx Only, Non-Sterile, UDI: (01)00190376268743
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0364 Insignia, ACP, 3-Level, 64 mm, Rx Only, Non-Sterile, UDI: (01)00190376268637
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0120, Insignia, ACP, 1-Level, 20 mm, Rx Only, Non-Sterile, UDI: (01)00190376268460
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0122, Insignia, ACP, 1-Level, 22 mm, Rx Only, Non-Sterile, UDI: (01)00190376268484
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0482 Insignia, ACP, 4-Level, 82 mm, Rx Only, Non-Sterile, UDI: (01)00190376268712
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0358 Insignia, ACP, 3-Level, 58 mm, Rx Only, Non-Sterile, UDI: (01)00190376268606
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0234 Insignia, ACP, 2-Level, 34 mm, Rx Only, Non-Sterile, UDI: (01)00190376268378
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0478 Insignia, ACP, 4-Level, 78 mm, Rx Only, Non-Sterile, UDI: (01)00190376268705
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0121, Insignia, ACP, 1-Level, 21 mm, Rx Only, Non-Sterile, UDI: (01)00190376268477
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0354 Insignia, ACP, 3-Level, 54 mm, Rx Only, Non-Sterile, UDI: (01)00190376268583
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0248 Insignia, ACP, 2-Level, 48 mm, Rx Only, Non-Sterile, UDI: (01)00190376268521
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0360 Insignia, ACP, 3-Level, 60 mm, Rx Only, Non-Sterile, UDI: (01)00190376268613
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0232 Insignia, ACP, 2-Level, 32 mm, Rx Only, Non-Sterile, UDI: (01)00190376268361
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0350 Insignia, ACP, 3-Level, 50 mm, Rx Only, Non-Sterile, UDI: (01)00190376268569
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI: (01)00190376268422
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Atec Insignia Anterior Cervical Plate System, REF 136-0238 Insignia, ACP, 2-Level, 38 mm, Rx Only, Non-Sterile, UDI: (01)00190376268392
  FDA Device · Class II · 2021-06-16 · Alphatec Spine
• Arsenal Spinal Fixation System, Set Screw, Part No. 47027 Product Usage: The Arsenal Spinal Fixation System is intended for posterior, non-…
  FDA Device · Class II · 2017-06-14 · Alphatec Spine
• Arsenal Spinal Fixation System, Set Screw, Part No. 47127 Product Usage: Usage: The Arsenal Spinal Fixation System is intended for posterio…
  FDA Device · Class II · 2016-11-23 · Alphatec Spine
• 4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 14mm Alphatec Spine Solutions for the Aging Spine Trestle Luxe Anterior Cervical Platin…
  FDA Device · Class II · 2015-05-06 · Alphatec Spine
• Solanas 2.1mm FIXED DEPTH DRILL, 10mm, Part No. 63928-10
  FDA Device · Class II · 2014-07-30 · Alphatec Spine
• Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm
  FDA Device · Class II · 2013-09-04 · Alphatec Spine
• Leucadia Autolok" Polyaxial Pedicle Screw System
  FDA Device · Class II · 2013-06-05 · Alphatec Spine
• ILLICO Straight CP TI Rod, -5.5MM x 110M
  FDA Device · Class II · 2013-03-27 · Alphatec Spine
• TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # 62065-55
  FDA Device · Class II · 2012-11-14 · Alphatec Spine
• ILLlCO¿ MIS Posterior Fixation System, Bone-screw Internal Spinal Fixation System, Orthosis, Spinal Pedical Fixation Orthosis, Spondylolist…
  FDA Device · Class II · 2012-11-07 · Alphatec Spine
• TRESTLE LUXE¿ Anterior Cervical Plating System, Product code KWQ. 510(k) K102820
  FDA Device · Class II · 2012-09-05 · Alphatec Spine