# FDA recall Z-1793-2022

> **Mckesson Medical-Surgical Inc. Corporate Office** · Class III · device recall initiated 2022-05-25.

## Product

a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model Number: LCB053.  b. STERIS CORP VERIFY Verify SixCess Sterilization Flash Indicator Strip Steam 2-3/4 Inch Model Number: PCC006.    c. STERIS CORP VERIFY Verify Sterilization Biological Indicator Pack Steam Model Number: S3069.    d.  STERIS CORP Celerity Celerity Sterilization Biological Indicator Vial Vaporized Hydrogen Peroxide Model Number:LCB044.    e. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model Number: LCB049.    f.  STERIS CORP VERIFY Sterilization Indicator Challenge Pack Steam Catalog #LCB035.

## Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1793-2022
- **Recalling firm:** Mckesson Medical-Surgical Inc. Corporate Office
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-25
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1793-2022

## Citation

> AI Analytics. FDA recall Z-1793-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1793-2022. Source: US FDA. Licensed CC0.

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