FDAClass IIAugust 6, 2025

Lyfo-disk recall

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

Why was Lyfo-disk recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

1) 0894L: UDI/DI 10845357021967, Lot Numbers 894-76-4 and 894-76-6

Product
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L
Recalling firm
Microbiologics Inc
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.
Recall date
August 6, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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