Microbiologics recalls LYFO-DISK products with REF 0894L lot numbers 894-76-4 and 894-76-6 due to potential failure to recover target microorganism. Affected users should check their product labels.
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.
Microbiologics is recalling LYFO-DISK products with specific lot numbers because they may fail to recover the target microorganism. This could impact laboratory results if used for microbiological testing.
The recalled LYFO-DISK products may not properly recover the target microorganism (M. Canis Derived from ATCC 36299) during laboratory testing. This could lead to inaccurate results if used for microbiological analysis.
Laboratory users who own or use LYFO-DISK products with REF 0894L lot numbers 894-76-4 and 894-76-6 are affected. Researchers and technicians working with microbiological samples are most at risk.
Check for REF 0894L packaging with lot numbers 894-76-4 or 894-76-6. The product is labeled as 'LYFO-DISK, M. Canis Derived from ATCC 36299'.
Look for REF 0894L with lot numbers 894-76-4 or 894-76-6 on the packaging.
The recalled product is LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as REF 0894L with lot numbers 894-76-4 and 894-76-6.
The product may result in failure to recover the target microorganism, which could impact laboratory results.
Check your product label for REF 0894L with lot numbers 894-76-4 or 894-76-6. The recall does not specify a remedy, so no action is required beyond verification.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-2195-2025 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-2195-2025 from Microbiologics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
