Alphatec Spine recalls

Alphatec Spine has 46 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 29 Jul 2026. 7 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls46since 2012

Last 12 months3reported

Class I00% of total

Ongoing7latest 29 Jul 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 1 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 2 0 0Apr 0 0 1Jul 0 0

Severity split

Class I 0 0%Class II 46 100%Class III 0 0%

Why alphatec spine is recalled

Product types

By year

202637%
202512%
202412%
202312%
202212%
20212963%
201712%
201612%
201512%
201412%

Ongoing alphatec spine recalls

7 active

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Device	CLASS II	SafeOp Patient Interface recalled by Alphatec Spine	Alphatec Spine	Device Malfunction	Nationwide
18 Feb 2026Device	CLASS II	Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled	Alphatec Spine	Sterility	Nationwide
18 Feb 2026Device	CLASS II	Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled	Alphatec Spine	Sterility	Nationwide
5 Feb 2025Device	CLASS II	Calibrate CCX Interbody System for spinal fusion procedures recalled	Alphatec Spine	Sterility	Nationwide
6 Mar 2024Device	CLASS II	IdentiTi ALIF Standalone Interbody System recalled by Alphatec Spine	Alphatec Spine	Device Malfunction	Nationwide
6 Sep 2023Device	CLASS II	LIF AMP, Adjustable Awl recalled by Alphatec Spine	Alphatec Spine	Lead & Heavy Metals	Nationwide

All alphatec spine recalls, newest first

46 total

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Device	CLASS II	SafeOp Patient Interface recalled by Alphatec Spine	Alphatec Spine	Device Malfunction	Nationwide
18 Feb 2026Device	CLASS II	Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled	Alphatec Spine	Sterility	Nationwide
18 Feb 2026Device	CLASS II	Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled	Alphatec Spine	Sterility	Nationwide
5 Feb 2025Device	CLASS II	Calibrate CCX Interbody System for spinal fusion procedures recalled	Alphatec Spine	Sterility	Nationwide
6 Mar 2024Device	CLASS II	IdentiTi ALIF Standalone Interbody System recalled by Alphatec Spine	Alphatec Spine	Device Malfunction	Nationwide
6 Sep 2023Device	CLASS II	LIF AMP, Adjustable Awl recalled by Alphatec Spine	Alphatec Spine	Lead & Heavy Metals	Nationwide
16 Nov 2022Device	CLASS II	Disc Preparation instruments contained recalled by Alphatec Spine	Alphatec Spine	Other	CA
16 Jun 2021Device	CLASS II	Atec Insignia Anterior Cervical Plate System recalled by Alphatec Spine	Alphatec Spine	Sterility	Nationwide
16 Jun 2021Device	CLASS II	Atec Insignia Anterior Cervical Plate System recalled by Alphatec Spine	Alphatec Spine	Sterility	Nationwide
16 Jun 2021Device	CLASS II	Atec Insignia Anterior Cervical Plate System recalled by Alphatec Spine	Alphatec Spine	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.