# FDA recall Z-0117-2022

> **Beckman Coulter Inc.** · Class II · device recall initiated 2021-07-28.

## Product

Power Processor 3K, 3K High Speed Stockyards  Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116

## Reason for recall

Missing splash guard which may expose users to hazardous materials. .

## Distribution

U.S. Nationwide Distribution in the states of: CA, GA, IA, ID, IL, IN, LA, MA, MI, MS, NJ, NY, OH, OR, PA, SC, SD, TN, TX, WA, and WV  O.U.S.: Canada, China, Spain, France, United Kingdom, Israel, Italy, South Korea, Kuwait, Lebanon, Mexico, Malaysia, Netherlands, Portugal, Qatar, Saudi Arabia, Thailand, Turkey, and Taiwan.  Additional O.U.S. added 12/15/2021 - South Africa

## Key facts

- **Recall number:** Z-0117-2022
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-07-28
- **Report date:** 2021-10-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brea, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0117-2022

## Citation

> AI Analytics. FDA recall Z-0117-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0117-2022. Source: US FDA. Licensed CC0.

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