Class II

Medical Device Recall: LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L

Microbiologics Inc · June 27, 2025

Reason for Recall

KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.

Distribution

Worldwide distribution - US Nationwide and the countries of France, Colombia, Philippines, Peru, Turkey, India, Finland, Trinidad and Tobago, Poland, Viet Nam, Brazil, Japan, Malaysia, Costa Rica.

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2195-2025

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.

Microbiologics Inc Medical Device Recall: LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L | SafeCheck