# FDA recall Z-2414-2024

> **Beckman Coulter, Inc.** · Class II · device recall initiated 2024-06-04.

## Product

Dxl 9000 Access Immunoassay Analyzer, Catalog #C11137.

## Reason for recall

The analyzers were built with nonconforming USB cables made with brass contacts instead of specified gold contacts.  Brass contacts may corrode over time, leading to loss of internal instrument communication and delayed patient results.

## Distribution

Worldwide - US Nationwide distribution in the states of FL, IN, KS, NH, PA, and TX. The countries of Australia, Austria, Belgium, Brazil, Croatia, Czechia, Egypt, France, Germany, Hungary, Ireland, Israel, Italy, Netherlands, New Zealand, Poland, Portugal, Slovakia, South Africa, Spain, Switzerland, Taiwan, Province of China, and United Kingdom of Great Britain and Northern Ireland.

## Key facts

- **Recall number:** Z-2414-2024
- **Recalling firm:** Beckman Coulter, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-04
- **Report date:** 2024-07-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chaska, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2414-2024

## Citation

> AI Analytics. FDA recall Z-2414-2024. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-2414-2024. Source: US FDA. Licensed CC0.

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