---
title: "KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805... — FDA record Z-2124-2025 | Is It on Recall"
description: "Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delay"
url: https://isitonrecall.com/recall/fda-device-z-2124-2025-kwik-stik-and-lyfo-disk-quality-control-kit-for-culture-media-catalog-0805k-and-0805l/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L — FDA record Z-2124-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 17, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Microbiologics Inc
- **Quantity**: 21 total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2124-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2124-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot #: 805-234-4, 805-234-5 UDI: (0805K) 30845357019531, (0805L) 10845357019544 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Ohio](https://isitonrecall.com/state/ohio/)
- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Jul 23, 2025
- **Recall initiation date**: Jun 17, 2025
- **Center classification date**: Jul 17, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2124-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Microbiologics Inc records](https://isitonrecall.com/brand/microbiologics-inc/)