# FDA recall Z-0205-2023

> **Carefusion 2200 Inc** · Class II · device recall initiated 2022-09-26.

## Product

CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD1-4ST

## Reason for recall

Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.

## 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

## Key facts

- **Recall number:** Z-0205-2023
- **Recalling firm:** Carefusion 2200 Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-26
- **Report date:** 2022-11-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vernon Hills, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0205-2023

## Citation

> AI Analytics. FDA recall Z-0205-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0205-2023. Source: US FDA. Licensed CC0.

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