# FDA recall Z-1609-2026

> **Beckman Coulter, Inc.** · Class II · device recall initiated 2025-07-24.

## Product

MicroScan Neg MIC 56 REF C42464  UDI-DI code: 15099590731212    MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.

## Reason for recall

Due to the likely presence of contamination in well(s).

## Distribution

U.S. Nationwide distribution in the states of CA, CO, IN, MA, MD, MN, MO, NC, NJ, OK, PA, and TX.

## Key facts

- **Recall number:** Z-1609-2026
- **Recalling firm:** Beckman Coulter, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-24
- **Report date:** 2026-04-01

- **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-1609-2026

## Citation

> AI Analytics. FDA recall Z-1609-2026. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-1609-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*