# FDA recall Z-1806-2026

> **Remel, Inc** · Class II · device recall initiated 2026-03-24.

## Product

Yeastone Broth, 11ML, 10/BOX  YY3462

## Reason for recall

Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.

## Key facts

- **Recall number:** Z-1806-2026
- **Recalling firm:** Remel, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-24
- **Report date:** 2026-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lenexa, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1806-2026

## Citation

> AI Analytics. FDA recall Z-1806-2026. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1806-2026. Source: US FDA. Licensed CC0.

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