# FDA recall Z-2576-2023

> **Microbiologics Inc** · Class III · device recall initiated 2023-08-14.

## Product

KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing

## Reason for recall

One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains, 6018P Parabacteroides distasonis.

## Distribution

US Nationwide distribution in the states of MN, PA, TN, TX.

## Key facts

- **Recall number:** Z-2576-2023
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-14
- **Report date:** 2023-09-20

- **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-2576-2023

## Citation

> AI Analytics. FDA recall Z-2576-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2576-2023. Source: US FDA. Licensed CC0.

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