Official recall record
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-
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2026-04-23
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- Novapproach Spine, LLC
What the authority reported
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
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-06-02.
Record last checked against the registry on 2026-06-02.
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