---
title: "regard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kit — FDA record Z-0302-2023 | Is It on Recall"
description: "Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled."
url: https://isitonrecall.com/recall/fda-device-z-0302-2023-regard-spine-nu00974f-item-number-800769006-neuro-surgery-convenience-kit/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# regard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kit — FDA record Z-0302-2023

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 20, 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**: regard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kit
- **Reason**: Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
- **Classification**: Class II
- **Recalling firm**: ROi CPS LLC
- **Quantity**: 21 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0302-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0302-2023%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 | UDI/DI 10194717114062, Lot Numbers: 91584, exp 9/23/2023 |

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

## Distribution

LA, MO, NC, FL

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)

## Dates in the source

- **Report date**: Nov 30, 2022
- **Recall initiation date**: Oct 20, 2022
- **Center classification date**: Nov 23, 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-0302-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ROi CPS LLC records](https://isitonrecall.com/brand/roi-cps-llc/)