---
title: "TRACH KIT W/HYDROGEN & SALI — FDA record Z-1044-2024 | Is It on Recall"
description: "Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist."
url: https://isitonrecall.com/recall/fda-device-z-1044-2024-trach-kit-w-hydrogen-sali/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TRACH KIT W/HYDROGEN & SALI — FDA record Z-1044-2024

Reported ongoing

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 Dec 4, 2023. 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**: TRACH KIT W/HYDROGEN & SALI
- **Reason**: Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
- **Classification**: Class I
- **Recalling firm**: Cardinal Health 200, LLC
- **Quantity**: 661,560 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1044-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1044-2024%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 | REF 47802; Lot Numbers: 2201103364, 2201103464, 2201804164, 2201804264, 2204627064, 2204627364, 2204801164, 2205309664, 2205309764, 2206020664, 2206020764, 2206731664, 2206731764, 2208117464, 2208117564, 2208828064, 2208828164, 2212326364, 2213014664, 2215107664, 2215808564, 2222816264, 2216523964, 2217209464, 2219323864, 2217915264, 2219326264, 2219910964, 2221312264, 2221312164, 2222816164, 2222816364, 2223528364, 2223528464, 2224243164, 2224243264, 2224929764, 2224929864, 2225515664, 2226320664, 2225515764, 2226320764, 2227034464, 2229112364, 2227725164, 2227725264, 2227022264, 2231226564, 2231914264, 2305711364, 2305711464, 2306201964, 2300121564, 2305706564, 2306622764, 2307909364, 2307305764, 2307305664, 2307909464, 2308600464, 2310101364, 2310101464, 2311517164, 2310900364 |

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

## Distribution

US and EMEA, Japan, Latin America

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Feb 28, 2024
- **Recall initiation date**: Dec 4, 2023
- **Center classification date**: Feb 16, 2024

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-1044-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cardinal Health 200, LLC records](https://isitonrecall.com/brand/cardinal-health-200-llc/)