# FDA recall Z-1772-2026

> **Beckman Coulter, Inc.** · Class II · device recall initiated 2025-06-25.

## Product

MicroScan Neg MIC 3J REF C54814

## Reason for recall

Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics

## Distribution

International distribution in the country of Japan.

## Key facts

- **Recall number:** Z-1772-2026
- **Recalling firm:** Beckman Coulter, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-25
- **Report date:** 2026-04-15

- **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-1772-2026

## Citation

> AI Analytics. FDA recall Z-1772-2026. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1772-2026. Source: US FDA. Licensed CC0.

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