# FDA recall Z-1736-2022

> **Steris Corporation Hopkins Facility** · Class III · device recall initiated 2022-08-10.

## Product

Verify SixCess Challenge Pack.  Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.

## Reason for recall

Product contains incorrect chemical indicators in packaging.

## Distribution

Distribution in the US only - AK, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MN, MO, MS, NE, NH, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, and WY

## Key facts

- **Recall number:** Z-1736-2022
- **Recalling firm:** Steris Corporation Hopkins Facility
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-08-10
- **Report date:** 2022-09-21
- **Termination date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1736-2022

## Citation

> AI Analytics. FDA recall Z-1736-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1736-2022. Source: US FDA. Licensed CC0.

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