# FDA recall Z-2124-2025

> **Microbiologics Inc** · Class II · device recall initiated 2025-06-17.

## Product

KWIK-STIK and LYFO DISK, quality control kit for culture media  Catalog # 0805K and 0805L

## Reason for recall

Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.

## Distribution

US distribution to states of: Utah and Ohio; and OUS (International) to countries of: Italy, Netherlands, Argentina, Korea, Jordan, Spain, and Bangladesh.

## Key facts

- **Recall number:** Z-2124-2025
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-17
- **Report date:** 2025-07-23

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2124-2025

## Citation

> AI Analytics. FDA recall Z-2124-2025. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2124-2025. Source: US FDA. Licensed CC0.

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