--- title: "Alphatec Spine, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Alphatec Spine, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/alphatec-spine-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Alphatec Spine, Inc. recall records **7** reported ongoing 7 records in this archive. Latest source date May 13, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 13, 2026 FDA device enforcement ### [SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System](https://isitonrecall.com/recall/fda-device-z-2793-2026-safeop-patient-interface-ref-aix11240-part-of-safeop-3-neural-informatix-system/) Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, a... Class II Reported ongoing Distribution: US Nationwide distribution in the states of TX, MO, IN. [Official source for SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2793-2026%22) Jan 2, 2026 FDA device enforcement ### [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 i...](https://isitonrecall.com/recall/fda-device-z-1342-2026-atec-lateral-navigation-disc-prep-instruments-lif-nav-osteotome-10mm-ref-266-01-000-10-n-udi-di-code/) Due a design issue where the navigated array connection geometry is incorrect. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AZ, CA, FL, IL, IN, MA, MI, MO, NC, NH, NY, TN, TX, and VA. [Official source for ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1342-2026%22) Jan 2, 2026 FDA device enforcement ### [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 i...](https://isitonrecall.com/recall/fda-device-z-1343-2026-atec-lateral-navigation-disc-prep-instruments-lif-nav-osteotome-10mm-ref-267-01-000-10-n-udi-di-code/) Due a design issue where the navigated array connection geometry is incorrect. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AZ, CA, FL, IL, IN, MA, MI, MO, NC, NH, NY, TN, TX, and VA. [Official source for ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1343-2026%22) Dec 15, 2024 FDA device enforcement ### [Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, nonsterile; (2) Calibrate CCX-O, 7 x 10 ...](https://isitonrecall.com/recall/fda-device-z-1065-2025-calibrate-ccx-interbody-system-for-spinal-fusion-procedures-implants-1-calibrate-ccx-o-7-x-10-x-25mm/) Complaints have been received regarding post-operative implant collapse. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, IN, MA, MD, MI, MN, NC, NJ, NY, OH, OK, OR, PA, SC, SD, TN, and UT. [Official source for Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1065-2025%22) Jan 26, 2024 FDA device enforcement ### [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 / IdentiTi ALIF SA Graft Bolt, 08.5 x ...](https://isitonrecall.com/recall/fda-device-z-1182-2024-identiti-alif-standalone-interbody-system-part-number-description-132-10-85-250-identiti-alif-sa-gra/) Due to reports of intraoperative graft bolt implantation breakages. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IN, KS, KY, MD, MI, MN, MS, NC, NH, NV, NY, OH, OK, OR, PA, Puerto Rico, ... [Official source for IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1182-2024%22) Jul 7, 2023 FDA device enforcement ### [LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF, Transcend LIF and Battalion LLIF,](https://isitonrecall.com/recall/fda-device-z-2475-2023-lif-amp-adjustable-awl-ref-117-165-part-of-the-amp-system-used-with-spine-lateral-interbody-systems/) Awl instrument adjustable drill button assembly assembled in the incorrect orientation, preventing locking feature from engaging with shaft at the desired set point; instruments lack ability to control awl depth by means of adjustable shaft advancement stop... Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, IN, TX, LA, OH, AL, NH, MA, NC, AZ, MD, NJ, IL, CA, UT, MI. [Official source for LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2475-2023%22) Sep 14, 2022 FDA device enforcement ### [Disc Preparation instruments contained in the following products: CI-11050-08102515 Longer IdentiTi PO Trial Tip, 11A X 8P X 10 X 25mm, 15¿ TC11050 00840180510810 CI-11050-09102...](https://isitonrecall.com/recall/fda-device-z-0196-2023-disc-preparation-instruments-contained-in-the-following-products-ci-11050-08102515-longer-identiti-p/) Due to manufacturing instruments which included additional features and adequate consideration was not given to the need for a new Regulatory filing. Class II Reported ongoing Distribution: U.S.: CA O.U.S.: N/A [Official source for Disc Preparation instruments contained in the following products: CI-11050-08102515 Longer Identi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0196-2023%22) ## Reasons in these listed records - Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring... - Due a design issue where the navigated array connection geometry is incorrect. - Complaints have been received regarding post-operative implant collapse. - Due to reports of intraoperative graft bolt implantation breakages. These examples come from this result page and are not a ranking of every recall reason. ## Checking Alphatec Spine, Inc. ### Is there a recall on alphatec spine, inc. right now? This archive contains 7 records, including 7 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Alphatec Spine, Inc.](https://isitonrecall.com/check/?q=Alphatec%20Spine%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)