---
title: "CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12\" (58.4 X 30.5CM) 4\"... — FDA record Z-0212-2023 | Is It on Recall"
description: "Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing."
url: https://isitonrecall.com/recall/fda-device-z-0212-2023-carefusion-v-mueller-genesis-full-length-container-23-x12-58-4-x-30-5cm-4-10cm-deep-sterrad-compatib/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3... — FDA record Z-0212-2023

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 Sep 26, 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**: CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST
- **Reason**: Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
- **Classification**: Class II
- **Recalling firm**: Carefusion 2200 Inc
- **Quantity**: 308 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0212-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0212-2023%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 (01) 10885403019319, ALL LOTS |

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

## Distribution

US and Australia, Bahrain, Canada, Denmark, Hong Kong, Italy, Japan, Malaysia, Mexico, Norway, Philippines, Saudi Arabia, Singapore, South Africa, Sweden, Thailand, UK, United Arab Emirates

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

## Dates in the source

- **Report date**: Nov 23, 2022
- **Recall initiation date**: Sep 26, 2022
- **Center classification date**: Nov 11, 2022

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-0212-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Carefusion 2200 Inc records](https://isitonrecall.com/brand/carefusion-2200-inc/)