Class II

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

Microbiologics Inc · June 17, 2025

Reason for Recall

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.

Distribution

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

Quantity Affected

21 total

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2124-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.