# FDA device recall: OneLIF Interbody Cage (REF/Description):  010-107-1007/Small 7 Degree 10mm X 7mm,  010-107-1007-2/Small 7 Degree 10mm X 

> recall · VERIFIED · 2026-04-23

Firm: Novapproach Spine, LLC · Class II · Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to 

- Company: Novapproach Spine, LLC
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED.