# FDA recall Z-1957-2025

> **Microbiologics Inc** · Class II · device recall initiated 2025-05-27.

## Product

KWIK-STICK, Quality control kit for culture media,     Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960;    0621K, Staphylococcus aureus derived from NCTC 12493

## Reason for recall

Affected products were packaged with the incorrect KWIK STIK assembly resulting in the product containing the wrong microorganism. 0621K was packaged 01065K swabs; 01065K was packaged with 0621K swabs. This may lead to delayed diagnosis.

## Distribution

US Nationwide distribution in the states of California and Pennsylvania and the country of New Zealand.

## Key facts

- **Recall number:** Z-1957-2025
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-27
- **Report date:** 2025-06-18

- **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-1957-2025

## Citation

> AI Analytics. FDA recall Z-1957-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1957-2025. Source: US FDA. Licensed CC0.

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