Reported Jul 23, 2025 · Ongoing

KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L

Microbiologics Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Microbiologics Inc · 200 Cooper Ave N · Saint Cloud, MN · 56303-4440

Is this the product you have?

  • KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L
Lot codes and dates
    • Lot #: 805-234-4
    • 805-234-5
  • UDI
    • (0805K) 30845357019531
    • (0805L) 10845357019544
Amount recalled
21 total

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.