FDAApril 23, 2026device

OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm, ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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 procedural delay and/or the need to select an alternative implant.

What to do

FDA enforcement status: Ongoing

Brands named

novapproach spinenovapproach

UPCs

01010710072010113100620102071007201030710062

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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