---
title: "OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-... — FDA record Z-0246-2023 | Is It on Recall"
description: "The torque limiting adapter may not stay locked inside of the ratcheting handle once fully engaged."
url: https://isitonrecall.com/recall/fda-device-z-0246-2023-onelif-torque-limiting-adapter-ao-to-1-4-sq-2-25nm-limit-catalog-015-010-0000-a-component-of-novappr/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine O... — FDA record Z-0246-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 12, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

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/).

## What the record says

- **Product**: OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine OneLIF Interbody System instrument kit, Catalog #OneLIF INS.
- **Reason**: The torque limiting adapter may not stay locked inside of the ratcheting handle once fully engaged.
- **Classification**: Class II
- **Recalling firm**: Novapproach Spine LLC
- **Quantity**: 6 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0246-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0246-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Torque adapter - Lot #104713, UDI G07001501000000; Kit IDs - 504, 505, 506, 501, 101, and 105. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution in the states of CA and NY.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Nov 23, 2022
- **Recall initiation date**: Oct 12, 2022
- **Center classification date**: Nov 17, 2022
- **Termination date**: Apr 1, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0246-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Novapproach Spine LLC records](https://isitonrecall.com/brand/novapproach-spine-llc/)
