# FDA recall Z-0269-2023

> **Beckman Coulter, Inc.** · Class II · device recall initiated 2022-10-03.

## Product

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

## Reason for recall

Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.

## Distribution

Worldwide - U.S. Nationwide distribution in the states of AK, FL, IA, ID, MI MS, MT, NC, NE, PA, SC, TX WA, WI, and WV. The countries of Chile, Germany, Indonesia, Italy, Japan, Mexico, Peru, Portugal, South Africa, Spain, United Kingdom of Great Britain and Northern Ireland, and Uruguay.

## Key facts

- **Recall number:** Z-0269-2023
- **Recalling firm:** Beckman Coulter, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-03
- **Report date:** 2022-11-30

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0269-2023

## Citation

> AI Analytics. FDA recall Z-0269-2023. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-0269-2023. Source: US FDA. Licensed CC0.

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