---
title: "Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother. — FDA record Z-1408-2022 | Is It on Recall"
description: "Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits."
url: https://isitonrecall.com/recall/fda-device-z-1408-2022-nonsterile-convenience-kit-regard-item-830014016-ld00199p-c-section-mother/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother. — FDA record Z-1408-2022

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 Jun 3, 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**: Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
- **Reason**: Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.
- **Classification**: Class II
- **Recalling firm**: ROi CPS LLC
- **Quantity**: 40 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1408-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1408-2022%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 | Lot #92605, exp. 8/31/2023, Item #830014016, UDI #10194717110156. |

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

## Distribution

Distribution was made to MO. There was no foreign/military/government distribution.

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

- [Missouri](https://isitonrecall.com/state/missouri/)

## Dates in the source

- **Report date**: Jul 27, 2022
- **Recall initiation date**: Jun 3, 2022
- **Center classification date**: Jul 19, 2022
- **Termination date**: Apr 14, 2023

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-1408-2022%22)

## Related records

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