# FDA recall Z-0787-2024

> **Beckman Coulter, Inc.** · Class II · device recall initiated 2023-12-19.

## Product

iQ Waste Well Adapter, Part Number:  700-3393

## Reason for recall

Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.

## Distribution

US and Australia, Brazil, Canada, China, France, Germany, Ghana, India, Israel, Italy, Lebanon, Lithuania, Mexico, Panama, Qatar, Romania, Saudi Arabia, Spain, Taiwan, Province of China, United Kingdom of Great Britain and Northern Ireland,

## Key facts

- **Recall number:** Z-0787-2024
- **Recalling firm:** Beckman Coulter, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-19
- **Report date:** 2024-01-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0787-2024

## Citation

> AI Analytics. FDA recall Z-0787-2024. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0787-2024. Source: US FDA. Licensed CC0.

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