# FDA recall Z-0641-2022

> **Microbiologics Inc** · Class III · device recall initiated 2013-03-25.

## Product

KWIK-STIK(TM), Quality control kit for culture media, sold as:     KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)

## Reason for recall

Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, South Africa, France, Netherlands, Mauritius, China.

## Key facts

- **Recall number:** Z-0641-2022
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2013-03-25
- **Report date:** 2022-02-23
- **Termination date:** 2022-04-22

- **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-0641-2022

## Citation

> AI Analytics. FDA recall Z-0641-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0641-2022. Source: US FDA. Licensed CC0.

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