# FDA recall Z-0511-2022

> **Microbiologics Inc** · Class II · device recall initiated 2020-12-16.

## Product

KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L;  Microsporum canis derived from ATCC 36299.

## Reason for recall

Contamination with S. epidermidis

## Distribution

Distribution was made to CA, IA,  IL, LA, MA, MI, NY, PA, SD, TN, VA, WI, and WV.  There was no government/military distribution.     Foreign distribution was made to Brazil, Canada, Colombia, Dominican Republic, Finland, France, India, Japan, Malaysia, Mexico, Netherlands, Poland, Romania, Saudi Arabia, Serbia, South Africa, and United Kingdom.

## Key facts

- **Recall number:** Z-0511-2022
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-16
- **Report date:** 2022-01-26
- **Termination date:** 2022-07-07

- **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-0511-2022

## Citation

> AI Analytics. FDA recall Z-0511-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0511-2022. Source: US FDA. Licensed CC0.

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